Long Qt Syndrome 5; Lqt5

Description

Congenital long QT syndrome is electrocardiographically characterized by a prolonged QT interval and polymorphic ventricular arrhythmias (torsade de pointes). These cardiac arrhythmias may result in recurrent syncope, seizure, or sudden death (Jongbloed et al., 1999).For a discussion of genetic heterogeneity of long QT syndrome, see LQT1 (OMIM ).

Clinical Features

Phenotypes and symptoms related to Long Qt Syndrome 5; Lqt5

  • Sudden cardiac death
  • Syncope
  • Ventricular fibrillation
  • Prolonged QT interval
  • Torsade de pointes

Incidence and onset information

— Based on the latest data available Long Qt Syndrome 5; Lqt5 have a estimated prevalence of 40 per 100k worldwide.


Mendelian

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Long Qt Syndrome 5; Lqt5 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Comprehensive Cardiac Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, RANGRF, MYPN, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6 , (...)

View the complete list with 87 more genes
Specificity
14 %
Genes
88 %
Cardiomyopathy Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

TMPO, TXNRD2, OBSCN, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2 , (...)

View the complete list with 92 more genes
Specificity
9 %
Genes
63 %
Comprehensive Arrhythmias Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

SCN4B, AKAP9, CASQ2, SNTA1, KCNE2, TRDN, CALM1, RYR2, ANK2, GPD1L, CACNB2, KCNE3, SCN3B, TRPM4, CACNA1C, KCNQ1, KCNE1, SCN5A, HCN4, SCN1B , (...)

View the complete list with 3 more genes
Specificity
53 %
Genes
75 %
Long QT Syndrome and Short QT Syndrome.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

SCN4B, AKAP9, SNTA1, KCNE2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
85 %
Genes
69 %
LQTS panel.

By Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS in Italy.

SCN4B, AKAP9, KCNE2, CALM2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
85 %
Genes
69 %
Cardiomyopathy and Arrhythmia Panel, Sequencing (85 Genes) and Deletion/Duplication (83 Genes).

By ARUP Laboratories, Molecular Genetics and Genomics in United States.

MYH10, CORIN, KLHL3, TMPO, OBSCN, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, TNNT2, TPM1, MYPN, JUP , (...)

View the complete list with 65 more genes
Specificity
12 %
Genes
63 %
Long QT Syndrome Sequencing Panel.

By GeneDx in United States.

SCN4B, AKAP9, SNTA1, KCNE2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
84 %
Genes
63 %
Long QT Syndrome Del/Dup Panel.

By GeneDx in United States.

SCN4B, AKAP9, SNTA1, KCNE2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
84 %
Genes
63 %
RhythmNext.

By Ambry Genetics in United States.

TBX5, DSC2, JUP, DSG2, NKX2-5, TGFB3, SCN4B, AKAP9, CASQ2, SNTA1, KCNE2, TRDN, CALM1, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B , (...)

View the complete list with 16 more genes
Specificity
34 %
Genes
75 %
RhythmFirst.

By Ambry Genetics in United States.

SCN4B, AKAP9, SNTA1, KCNE2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
84 %
Genes
63 %
RhythmFirst reflex RhythmNext.

By Ambry Genetics in United States.

TBX5, DSC2, JUP, DSG2, NKX2-5, TGFB3, SCN4B, AKAP9, CASQ2, SNTA1, KCNE2, TRDN, CALM1, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B , (...)

View the complete list with 16 more genes
Specificity
34 %
Genes
75 %
Long QT syndrome 10 (sequence analysis of SCN4B gene).

By CGC Genetics in Portugal.

SCN4B
Specificity
100 %
Genes
7 %
Cardiomyopathy and changes in cardiac conduction (NGS panel for 59 genes).

By CGC Genetics in Portugal.

TNNI3K, ALG10, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, TNNT2, TPM1, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1 , (...)

View the complete list with 39 more genes
Specificity
23 %
Genes
82 %
Long QT Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, CALM2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
87 %
Genes
82 %
Comprehensive Cardiology Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

ZBTB17, SREBF2, TRIM63, ZHX3, KLF10, TBX3, CALR3, MIB1, CAVIN4, CREB3L3, APOA4, GJA5, NPPA, GPIHBP1, APOC2, LMF1, LPL, APOA5, LDLRAP1, CETP , (...)

View the complete list with 144 more genes
Specificity
8 %
Genes
82 %
Cardiac channelopathy Deletion/ Duplication panel.

By Connective Tissue Gene Tests in United States.

TECRL, KCND2, CALM3, KCNE5, SCN10A, FGF12, SEMA3A, NOS1AP, RANGRF, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2 , (...)

View the complete list with 21 more genes
Specificity
40 %
Genes
100 %
Cardiac channelopathy Comprehensive panel.

By Connective Tissue Gene Tests in United States.

TECRL, KCND2, CALM3, KCNE5, SCN10A, FGF12, SEMA3A, NOS1AP, RANGRF, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2 , (...)

View the complete list with 21 more genes
Specificity
40 %
Genes
100 %
Long QT syndrome Comprehensive panel.

By Connective Tissue Gene Tests in United States.

CALM3, NOS1AP, SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
79 %
Genes
94 %
Long QT syndrome NGS panel.

By Connective Tissue Gene Tests in United States.

CALM3, NOS1AP, SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
79 %
Genes
94 %
Heart Diseases - panels.

By MGZ Medical Genetics Center in Germany.

TLL1, NKX2-6, NR2F2, MED13L, TAB2, SMAD6, TBX20, GATA5, ADAMTSL4, ZFPM2, NOTCH2, CFC1, GATA6, CRELD1, CITED2, GATA4, GDF1, GJA1, TBX5, VCL , (...)

View the complete list with 137 more genes
Specificity
9 %
Genes
88 %
Long QT syndrome panel.

By Centogene AG - the Rare Disease Company in Germany.

SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
85 %
Genes
69 %
Arrhythmia, familial panel.

By Centogene AG - the Rare Disease Company in Germany.

NPPA, DSC2, JUP, DSG2, PLN, TGFB3, KCNA5, SCN4B, AKAP9, CASQ2, SNTA1, KCNE2, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, CACNA1C , (...)

View the complete list with 9 more genes
Specificity
35 %
Genes
63 %
Long QT Syndrome Panel.

By CeGaT GmbH in Germany.

SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, CALM2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
87 %
Genes
82 %
Cardio-channelopathy-gene-panel.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

GJA5, NPPA, GJA1, DPP6, KCNA5, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM1, RYR2, ANK2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B , (...)

View the complete list with 13 more genes
Specificity
40 %
Genes
82 %
Arrhythmia.

By Asper Biogene Asper Biogene LLC in Estonia.

GJA5, NPPA, DSC2, JUP, DSG2, PLN, NKX2-5, TGFB3, KCNA5, SCN4B, AKAP9, CASQ2, SNTA1, KCNE2, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3 , (...)

View the complete list with 18 more genes
Specificity
27 %
Genes
63 %
SCN4B gene sequencing.

By Health in Code in Spain.

SCN4B
Specificity
100 %
Genes
7 %
Long QT Syndrome Extended Panel.

By Health in Code in Spain.

KCNE5, FHL2, KCNA5, SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, CALM2, CALM1, RYR2, ANK2, KCNE3, CACNA1C, KCNQ1, KCNE1, SCN5A, HCN4, SCN1B, KCNH2 , (...)

View the complete list with 3 more genes
Specificity
57 %
Genes
82 %
Inherited Cardiovascular Diseases and Sudden Death Panel.

By Health in Code in Spain.

FHOD3, FOXD4, SMAD1, TRIM63, KLF10, LRP6, CALR3, MIB1, TBX20, CAVIN4, APOC3, ADAMTSL4, KCNE5, CTNNA3, SCN10A, OBSL1, ANK3, AGPAT2, GJA5, NPPA , (...)

View the complete list with 193 more genes
Specificity
8 %
Genes
94 %
Ventricular arrhythmia and sudden death without structural heart disease.

By Health in Code in Spain.

IRX3, KCNK17, KCND2, TNNI3K, CALM3, CAVIN4, KCNE5, SCN10A, FGF12, ANK3, GJA5, NPPA, FHL2, TBX5, NOS1AP, DSC2, TNNT2, RANGRF, JUP, DSG2 , (...)

View the complete list with 57 more genes
Specificity
21 %
Genes
100 %
Cardiovascular Diseases_General Panel.

By Health in Code in Spain.

CH25H, BMP10, TRIB1, TOPBP1, ISL1, GREM2, HAND2, SLC25A40, NNT, PPARA, MYOM1, LPA, SLC22A8, IRX3, KCNK17, PPP1R13L, PERP, FHOD3, FOXD4, SMAD1 , (...)

View the complete list with 360 more genes
Specificity
5 %
Genes
100 %
Cardiac conduction disease Panel.

By Health in Code in Spain.

IRX3, KCNK17, TNNI3K, CAVIN4, SCN10A, GJA5, NPPA, TBX5, PRKAG2, MYH6, NKX2-5, ACTC1, SCN4B, KCNE2, TRPM4, LAMP2, KCNQ1, CACNA1D, SCN5A, HCN4 , (...)

View the complete list with 14 more genes
Specificity
18 %
Genes
38 %
Atrial fibrillation Panel.

By Health in Code in Spain.

GREM2, NKX2-6, TNNI3K, GATA5, KCNE5, SCN10A, GJA5, NPPA, GATA6, GATA4, GJA1, TBX5, JPH2, TNNT2, TPM1, TNNI3, NKX2-5, ACTC1, KCNA5, KCNK3 , (...)

View the complete list with 23 more genes
Specificity
19 %
Genes
50 %
Arrhythmia General Panel.

By Health in Code in Spain.

GREM2, NNT, MYOM1, IRX3, KCNK17, PPP1R13L, PERP, FHOD3, FOXD4, NKX2-6, MRPL44, KCND2, COA6, TRIM63, KLF10, PKP4, TNNI3K, CALM3, CALR3, MIB1 , (...)

View the complete list with 198 more genes
Specificity
8 %
Genes
100 %
Arrhythmias: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

CTNNA3, GJA5, NPPA, DSC2, RANGRF, JUP, DSG2, NKX2-5, KCNA5, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM1, RYR2, ANK2, PKP2 , (...)

View the complete list with 17 more genes
Specificity
33 %
Genes
75 %
Long and Short QT Syndrome: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

SCN4B, AKAP9, SNTA1, KCNE2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
84 %
Genes
63 %
Comprehensive Cardiovascular: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

TMPO, FHL2, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, RANGRF, MYPN, JUP, DSG2, NEXN , (...)

View the complete list with 86 more genes
Specificity
11 %
Genes
69 %
Long QT syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
85 %
Genes
69 %
Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

EFHC2, CELSR1, GPHN, SLC6A5, GLRA1, GLRB, SCN10A, BUB1B, MAPK10, COL18A1, ACY1, MED17, SNAP29, LIG4, NHEJ1, SLC46A1, ARL13B, RPGRIP1L, PGK1, SCN4B , (...)

View the complete list with 323 more genes
Specificity
1 %
Genes
19 %
SCN4B.

By Fulgent Genetics Fulgent Genetics in United States.

SCN4B
Specificity
100 %
Genes
7 %
Comprehensive Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

RANGAP1, EFHC2, CELSR1, NIPA2, UBR5, VDAC1, BRD2, RBFOX3, KPNA7, CNTN2, ARHGEF15, PIK3AP1, FASN, RYR3, GABBR2, HCN2, TNK2, SRGAP2, GPHN, SLC12A5 , (...)

View the complete list with 427 more genes
Specificity
1 %
Genes
25 %
Arrhythmia Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, CALM1, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, KCNJ8, CACNA1C, KCNQ1, KCNE1, SCN5A, HCN4 , (...)

View the complete list with 5 more genes
Specificity
48 %
Genes
75 %
Long QT Syndrome Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
85 %
Genes
69 %
Long QT Syndrome NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

CALM3, SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, TRDN, CALM1, RYR2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
77 %
Genes
82 %
SCN4B Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

SCN4B
Specificity
100 %
Genes
7 %
Cardiac Arrhythmia Exome Panel.

By Northwest Clinical Genomics Laboratory University of Washington in United States.

GNAI2, GJA5, NPPA, DPP6, DSC2, RBM20, TNNT2, DSG2, PLN, PRKAG2, MYH6, NKX2-5, KCNA5, SCN4B, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM2 , (...)

View the complete list with 31 more genes
Specificity
26 %
Genes
82 %
Long QT Syndrome Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, CALM2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
87 %
Genes
82 %
Ventricular Fibrillation, Familial Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, CALM2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
87 %
Genes
82 %
Long QT Syndrome , Panel Massive Sequencing (NGS) 11 Genes.

By Reference Laboratory Genetics in Spain.

SCN4B, AKAP9, SNTA1, KCNE2, ANK2, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
91 %
Genes
63 %
Familial Atrial Fibrillation , Panel Massive Sequencing (NGS) 13 Genes.

By Reference Laboratory Genetics in Spain.

GJA5, NPPA, NUP155, KCNA5, SCN4B, KCNE2, SCN3B, SCN2B, ABCC9, KCNQ1, SCN5A, SCN1B, KCNJ2
Specificity
31 %
Genes
25 %
Ventricular Arrhythmia and Sudden Cardiac Death , Panel Massive Sequencing (NGS) 48 Genes.

By Reference Laboratory Genetics in Spain.

CTNNA3, SCN10A, DSC2, TNNT2, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM1, RYR2 , (...)

View the complete list with 28 more genes
Specificity
30 %
Genes
88 %
Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes.

By Reference Laboratory Genetics in Spain.

ECE1, CTNNA3, CACNA1G, GJA5, NPPA, NUP155, SLC6A4, GJA1, DPP6, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, TNNT2, TPM1 , (...)

View the complete list with 75 more genes
Specificity
14 %
Genes
82 %
Phosphorus Pan Arrhythmia Panel.

By Phosphorus Diagnostics LLC in United States.

CALM3, SCN10A, DSC2, ACTN2, RBM20, TNNT2, JUP, DSG2, PLN, PRKAG2, TNNI3, TGFB3, SCN4B, CASQ2, SNTA1, KCNE2, TRDN, CALM2, CALM1, RYR2 , (...)

View the complete list with 22 more genes
Specificity
31 %
Genes
82 %
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Rasopathies Panel.

By Phosphorus Diagnostics LLC in United States.

CALM3, SCN10A, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, SCN4B , (...)

View the complete list with 67 more genes
Specificity
15 %
Genes
82 %
Long QT Syndrome: gene sequencing panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, CALM2, CALM1, ANK2, CACNA1C, KCNE1, KCNJ2, CAV3
Specificity
84 %
Genes
63 %
Long QT Syndrome Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
78 %
Genes
88 %
Long QT Syndrome Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
86 %
Genes
75 %
Cardiac Channelopathy Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

RANGRF, KCNA5, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM1, RYR2, ANK2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, ABCC9, KCNJ8, SLMAP , (...)

View the complete list with 12 more genes
Specificity
41 %
Genes
82 %
SCN4B.

By Institute for Human Genetics University Clinic Freiburg in Germany.

SCN4B
Specificity
100 %
Genes
7 %
Comprehensive Arrhythmia Panel.

By GeneDx in United States.

DSC2, RANGRF, JUP, DSG2, NKX2-5, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, KCNJ8, CACNA1C , (...)

View the complete list with 10 more genes
Specificity
37 %
Genes
69 %
Long QT Syndrome Gene Sequencing & Del/Dup Panel.

By GeneDx in United States.

SCN4B, AKAP9, SNTA1, KCNE2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
84 %
Genes
63 %
CardioNext with TTN.

By Ambry Genetics in United States.

TBX20, GATA4, TMPO, TXNRD2, TBX5, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2 , (...)

View the complete list with 65 more genes
Specificity
16 %
Genes
82 %
CustomNext: Cardio.

By Ambry Genetics in United States.

TBX20, GATA4, TMPO, TXNRD2, TBX5, PRKG1, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP , (...)

View the complete list with 86 more genes
Specificity
13 %
Genes
82 %
Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

CALM3, ASPH, KCNE5, SCN10A, GJA5, NPPA, DPP6, TNNT2, RANGRF, PLN, PRKAG2, KCNA5, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM2 , (...)

View the complete list with 27 more genes
Specificity
32 %
Genes
94 %
Cardiac conduction changes (NGS panel for 27 genes).

By CGC Genetics in Portugal.

TNNI3K, ALG10, PRKAG2, MYH6, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM1, RYR2, ANK2, GPD1L, CACNB2, KCNE3, SCN3B, CACNA1C, KCNQ1 , (...)

View the complete list with 7 more genes
Specificity
49 %
Genes
82 %
Long QT syndrome (NGS panel for 14 genes).

By CGC Genetics in Portugal.

ALG10, SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
79 %
Genes
69 %
Long QT Syndrome via SCN4B Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

SCN4B
Specificity
100 %
Genes
7 %
Sudden Cardiac Arrest Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MYL3, MYL2, DSC2, CSRP3, ACTN2, JPH2, TNNT2, TPM1, JUP, DSG2, NEXN, MYH6, TNNI3, TNNC1, MYLK2, KCNA5, SCN4B, AKAP9, CASQ2, SNTA1 , (...)

View the complete list with 29 more genes
Specificity
23 %
Genes
69 %
Comprehensive Cardiac Arrhythmia Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MYL4, TNNI3K, CALM3, KCNE5, SCN10A, GJA5, NPPA, DSC2, RANGRF, JUP, DSG2, PLN, PRKAG2, MYH6, TNNI3, NKX2-5, TGFB3, KCNA5, KCNK3, SCN4B , (...)

View the complete list with 35 more genes
Specificity
28 %
Genes
94 %
Cardiac channelopathy NGS panel.

By Connective Tissue Gene Tests in United States.

TECRL, KCND2, CALM3, KCNE5, SCN10A, FGF12, SEMA3A, NOS1AP, RANGRF, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2 , (...)

View the complete list with 21 more genes
Specificity
40 %
Genes
100 %
Long QT syndrome Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

CALM3, NOS1AP, SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
79 %
Genes
94 %
Cardiac conduction abnormalities panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

DSC2, JUP, DSG2, PLN, TGFB3, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, KCNJ8, KCNQ1 , (...)

View the complete list with 13 more genes
Specificity
34 %
Genes
69 %
Long QT syndrome type 10.

By Centogene AG - the Rare Disease Company in Germany.

SCN4B
Specificity
100 %
Genes
7 %
Atrial Fibrillation and Short QT Syndrome Panel.

By CeGaT GmbH in Germany.

GJA5, NPPA, KCNA5, SCN4B, KCNE2, CACNB2, SCN3B, SCN2B, ABCC9, CACNA1C, KCNQ1, KCNE1, CACNA2D1, SCN5A, SCN1B, KCNH2, KCNJ2
Specificity
36 %
Genes
38 %
Long QT Syndrome 10.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN4B
Specificity
100 %
Genes
7 %
Long QT Syndrome.

By Asper Biogene Asper Biogene LLC in Estonia.

SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
86 %
Genes
75 %
Standard Long QT syndrome Stage 2.

By Health in Code in Spain.

SCN4B, KCNJ2, CAV3
Specificity
67 %
Genes
13 %
Auricular Fibrillation Panel.

By Health in Code in Spain.

KCNE5, SCN10A, GJA5, NPPA, GATA6, GATA4, GJA1, TBX5, JPH2, TNNT2, TPM1, TNNI3, NKX2-5, ACTC1, KCNA5, KCNK3, SCN4B, KCNJ5, KCNE2, RYR2 , (...)

View the complete list with 18 more genes
Specificity
22 %
Genes
50 %
Ventricular Arrythmia & Sudden Death Panel with Structural Heart Disease.

By Health in Code in Spain.

FHOD3, TRIM63, KLF10, CALR3, CAVIN4, KCNE5, CTNNA3, SCN10A, OBSL1, ANK3, AGPAT2, GJA5, NPPA, GATA6, GATA4, FHL2, CTF1, GJA1, TBX5, VCL , (...)

View the complete list with 121 more genes
Specificity
11 %
Genes
94 %
Cardiac Conduction Disease Panel.

By Health in Code in Spain.

CAVIN4, SCN10A, GJA5, NPPA, TBX5, PRKAG2, MYH6, NKX2-5, ACTC1, SCN4B, KCNE2, TRPM4, LAMP2, KCNQ1, CACNA1D, SCN5A, HCN4, SCN1B, KCNH2, EMD , (...)

View the complete list with 8 more genes
Specificity
22 %
Genes
38 %
Ventricular Arrythmia & Sudden Death Panel without Structural Heart Disease.

By Health in Code in Spain.

KCNE5, CTNNA3, SCN10A, ANK3, DSC2, TNNT2, RANGRF, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, TRDN , (...)

View the complete list with 33 more genes
Specificity
29 %
Genes
94 %
Long QT Syndrome Extended Panel.

By Health in Code in Spain.

KCND2, CALM3, KCNE5, FHL2, NOS1AP, KCNA5, SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2, KCNE3, CACNA1C, KCNQ1, KCNE1 , (...)

View the complete list with 8 more genes
Specificity
54 %
Genes
94 %
LONG QT SYNDROME.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KCNE5, FHL2, NOS1AP, KCNA5, SCN4B, AKAP9, SNTA1, KCNJ5, KCNE2, TRDN, CALM1, RYR2, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, HCN4, SCN1B, KCNH2 , (...)

View the complete list with 3 more genes
Specificity
61 %
Genes
88 %
Comprehensive Cardiovascular: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

CTNNA3, GJA5, NPPA, TMPO, FHL2, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, RANGRF, MYPN , (...)

View the complete list with 97 more genes
Specificity
12 %
Genes
82 %
Arrhythmias: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

DSC2, RANGRF, JUP, DSG2, NKX2-5, SCN4B, AKAP9, CASQ2, SNTA1, KCNJ5, KCNE2, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, KCNJ8, CACNA1C , (...)

View the complete list with 9 more genes
Specificity
35 %
Genes
63 %
Familial Arrhythmia Full Gene Sequencing Panel.

By Integrated Genetics Westborough Integrated Genetics in United States.

ATP1B1, GINS3, LIG3, NPPA, NOS1AP, DSC2, JUP, DSG2, PLN, TGFB3, SCN4B, AKAP9, CASQ2, SNTA1, KCNE2, RYR2, ANK2, PKP2, GPD1L, CACNB2 , (...)

View the complete list with 10 more genes
Specificity
37 %
Genes
69 %
Arrhythmia NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

GYG1, GJA5, NPPA, DSC2, JUP, DSG2, PRKAG2, TGFB3, KCNA5, SCN4B, AKAP9, CASQ2, SNTA1, KCNE2, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3 , (...)

View the complete list with 18 more genes
Specificity
27 %
Genes
63 %
Pan-Cardio NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MYOM1, CALR3, CAVIN4, GJA5, NPPA, GATA4, TMPO, TXNRD2, CTF1, TBX5, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2 , (...)

View the complete list with 81 more genes
Specificity
11 %
Genes
69 %
Atrial Fibrillation NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

GJA5, NPPA, NUP155, GATA6, GATA4, KCNA5, SCN4B, KCNJ5, KCNE2, RYR2, SCN3B, SCN2B, ABCC9, KCNJ8, KCNQ1, KCNE1, SCN5A, HCN4, SCN1B, KCNH2 , (...)

View the complete list with 3 more genes
Specificity
31 %
Genes
44 %
Sudden Death Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

LRP6, CALR3, GJA5, NPPA, TMPO, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, RBM20, MYOZ2, JPH2, TNNT2, TPM1, JUP, DSG2, NEXN , (...)

View the complete list with 48 more genes
Specificity
15 %
Genes
63 %
Long QT syndrome type X.

By Bioarray in Spain.

SCN4B
Specificity
100 %
Genes
7 %
CardioGene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

TMPO, FHL2, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, GATAD1, TNNT2, TPM1, JUP, DSG2, NEXN, PLN, PRKAG2 , (...)

View the complete list with 60 more genes
Specificity
15 %
Genes
75 %
SCN4B Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

SCN4B
Specificity
100 %
Genes
7 %
Phosphorus Pan Arrhythmia and Cardiomyopathy Panel.

By Phosphorus Diagnostics LLC in United States.

CALM3, SCN10A, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, SCN4B , (...)

View the complete list with 50 more genes
Specificity
19 %
Genes
82 %
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

CALM3, SCN10A, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, SCN4B , (...)

View the complete list with 75 more genes
Specificity
14 %
Genes
82 %
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

CALM3, SCN10A, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, SCN4B , (...)

View the complete list with 58 more genes
Specificity
17 %
Genes
82 %
Phosphorus Long QT Syndrome Panel.

By Phosphorus Diagnostics LLC in United States.

CALM3, SCN4B, SNTA1, KCNE2, TRDN, CALM2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
80 %
Genes
75 %
Hearing Loss Advanced Sequencing and CNV Evaluation.

By Athena Diagnostics Inc in United States.

GRXCR2, SYNE4, ELMOD3, TMEM132E, EPS8L2, OTOGL, CEACAM16, DIAPH3, POLR1D, TPRN, GRXCR1, LOXHD1, TSPEAR, NARS2, TRIOBP, TMIE, TFAP2A, TJP2, S1PR2, SLC26A5 , (...)

View the complete list with 151 more genes
Specificity
2 %
Genes
13 %
NGS Hearing Loss Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

MITF, CATSPER2, GPSM2, MT-RNR1, CEACAM16, TPRN, GRXCR1, LOXHD1, TSPEAR, TRIOBP, TMIE, TJP2, SLC26A5, POU4F3, OTOA, MYH9, MYH14, LHFPL5, LRTOMT, GJB3 , (...)

View the complete list with 71 more genes
Specificity
3 %
Genes
13 %
Hearing Loss Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MASP1, MYO1A, DTD1, SLC29A3, SALL4, MITF, GPSM2, MT-RNR1, RPS6KA3, CEACAM16, DIAPH3, TPRN, GRXCR1, LOXHD1, TRIOBP, TMIE, TJP2, SLC26A5, SEMA3E, POU4F3 , (...)

View the complete list with 102 more genes
Specificity
2 %
Genes
13 %
LQT Multi-Gene Package.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

KCNE2, KCNQ1, KCNE1, SCN5A, KCNH2
Specificity
100 %
Genes
32 %
KCNH2, KCNQ1, SCN5A. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

KCNQ1, SCN5A, KCNH2
Specificity
100 %
Genes
19 %
Audiome (hearing loss panel).

By Division of Genomic Diagnostics The Children's Hospital of Philadelphia in United States.

SLC52A3, SLC52A2, MITF, GPSM2, GRXCR2, SYNE4, OTOGL, CEACAM16, TPRN, GRXCR1, LOXHD1, TSPEAR, TRIOBP, TMIE, S1PR2, POU4F3, OTOA, MYH9, LHFPL5, LRTOMT , (...)

View the complete list with 86 more genes
Specificity
2 %
Genes
13 %
Jervell and Lange-Nielsen syndrome (NGS panel of 2 genes).

By CGC Genetics in Portugal.

KCNQ1, KCNE1
Specificity
100 %
Genes
13 %
Long QT syndrome.

By Unit for Cardiac and Cardiavasular Genetics Oslo University Hospital HF - Ullevaal in Norway.

KCNE2, KCNQ1, KCNE1, SCN5A, KCNH2
Specificity
100 %
Genes
32 %
Familial Atrial Fibrillation Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

KCNE5, GJA5, NPPA, KCNA5, KCNE2, SCN3B, SCN2B, ABCC9, KCNQ1, KCNE1, SCN5A, SCN1B, KCNH2, KCND3, KCNJ2
Specificity
34 %
Genes
32 %
Catecholaminergic Polymorphic Ventricular Tachycardia Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

CASQ2, TRDN, CALM1, RYR2, ANK2, KCNQ1, SCN5A, KCNJ2
Specificity
63 %
Genes
32 %
Fetal Concerns Sequencing Panel Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

GLE1, CHRNG, KAT6B, PEX12, PEX10, PEX26, PEX6, KCNQ1, SCN5A, KCNH2, CHRND, CHRNA1, MUSK, KLHL40, RAPSN, SUMF1, SLC17A5, PEX1, DOK7, CBL , (...)

View the complete list with 20 more genes
Specificity
8 %
Genes
19 %
Long QT Syndrome (LQTS).

By MGZ Medical Genetics Center in Germany.

KCNE2, RYR2, KCNQ1, KCNE1, KCNH2, CAV3
Specificity
84 %
Genes
32 %
Long QT syndrome.

By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München in Germany.

KCNE2, KCNQ1, KCNE1, SCN5A, KCNH2
Specificity
100 %
Genes
32 %
Long QT syndrome type 1.

By Centogene AG - the Rare Disease Company in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
Short QT syndrome type 2.

By Centogene AG - the Rare Disease Company in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
CentoICU platinum plus.

By Centogene AG - the Rare Disease Company in Germany.

OPLAH, PPM1K, IKBKB, LCK, CABS1, SOX6, OPRM1, IL2, CTPS1, IRF8, CD247, ADK, UQCC2, MPC1, UPB1, CORO1A, CD3G, MCM4, UQCRC2, GPHN , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
32 %
CentoICU platinum.

By Centogene AG - the Rare Disease Company in Germany.

FRAS1, TSPYL1, IL2RA, CARD11, NOTCH2, TNFRSF13C, PRKDC, ICOS, CD81, CR2, CD19, F7, JAGN1, ABCC2, NFKB2, IL12RB1, COL7A1, COL17A1, ITGA6, ITGB4 , (...)

View the complete list with 494 more genes
Specificity
1 %
Genes
32 %
Syndromic Hearing Loss Panel.

By CeGaT GmbH in Germany.

MITF, POLR1D, TFAP2A, SEMA3E, GATA3, FOXI1, FGF3, CHSY1, SLITRK6, SIX1, KCNQ1, KCNE1, TCOF1, SLC19A2, SOX10, SNAI2, SIX5, EDNRB, PAX3, NLRP3 , (...)

View the complete list with 42 more genes
Specificity
4 %
Genes
13 %
Long QT syndrome 1.

By Innovagenomics Innovagenomics S.L in Spain.

KCNQ1
Specificity
100 %
Genes
7 %
Short QT Syndrome 2.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
Jervell and Lange-Nielson Syndrome.

By Asper Biogene Asper Biogene LLC in Estonia.

KCNQ1, KCNE1
Specificity
100 %
Genes
13 %
Long QT syndrome, KCNQ1 sequencing.

By Molecular Diagnostics Laboratory Seoul National University Hospital in South Korea.

KCNQ1
Specificity
100 %
Genes
7 %
KCNQ1 gene sequencing.

By Health in Code in Spain.

KCNQ1
Specificity
100 %
Genes
7 %
Left Ventricular Non-Compactation Panel.

By Health in Code in Spain.

MIB1, DTNA, MYL3, MYL2, CSRP3, ACTN2, TNNT2, TPM1, PLN, MYH6, TNNI3, TNNC1, ANKRD1, NKX2-5, PRDM16, ACTC1, CASQ2, RYR2, NOTCH1, KCNQ1 , (...)

View the complete list with 16 more genes
Specificity
6 %
Genes
13 %
Long QT Syndrome Short Panel.

By Health in Code in Spain.

KCNE2, RYR2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2
Specificity
63 %
Genes
32 %
Cardiomyopathies Panel.

By Health in Code in Spain.

FHOD3, FOXD4, TRIM63, KLF10, CALR3, MIB1, TBX20, CAVIN4, CTNNA3, OBSL1, AGPAT2, GJA5, GATA6, CRELD1, GATA4, TMPO, TXNRD2, FHL2, CTF1, GJA1 , (...)

View the complete list with 129 more genes
Specificity
4 %
Genes
32 %
Long QT Syndrome Panel.

By Health in Code in Spain.

KCNE2, RYR2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2
Specificity
63 %
Genes
32 %
Non-compaction cardiomyopathy.

By Health in Code in Spain.

NNT, MIB1, DTNA, MYL3, MYL2, CSRP3, ACTN2, TNNT2, TPM1, PLN, MYH6, TNNI3, TNNC1, ANKRD1, NKX2-5, PRDM16, ACTC1, CASQ2, RYR2, NOTCH1 , (...)

View the complete list with 17 more genes
Specificity
6 %
Genes
13 %
Short QT syndrome.

By Health in Code in Spain.

CACNB2, CACNA1C, KCNQ1, CACNA1D, CACNA2D1, KCNH2, KCNJ2
Specificity
29 %
Genes
13 %
Short QT Syndrome 2.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

KCNQ1
Specificity
100 %
Genes
7 %
KCNQ1-Related Familial Atrial Fibrillation.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

KCNQ1
Specificity
100 %
Genes
7 %
Long QT Syndrome 1.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

KCNQ1
Specificity
100 %
Genes
7 %
Invitae Arrhythmia Comprehensive Panel.

By Invitae in United States.

MYL4, CALM3, DSC2, ACTN2, RBM20, TNNT2, JUP, DSG2, PLN, PRKAG2, TNNI3, NKX2-5, KCNA5, CASQ2, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2 , (...)

View the complete list with 19 more genes
Specificity
26 %
Genes
63 %
Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel.

By Invitae in United States.

MYL4, CALM3, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, NKX2-5, TGFB3, ACTC1 , (...)

View the complete list with 47 more genes
Specificity
15 %
Genes
63 %
Invitae Long QT Syndrome Panel.

By Invitae in United States.

CALM3, KCNE2, TRDN, CALM2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
77 %
Genes
63 %
Invitae Short QT Syndrome Panel.

By Invitae in United States.

CACNB2, CACNA1C, KCNQ1, KCNH2, KCNJ2
Specificity
40 %
Genes
13 %
Russell-Silver syndrome: Methylation detection and deletions-duplications analysis (MLPA) (KvDMR / H19DMR domains).

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

IGF2, KCNQ1OT1, H19, KCNQ1, CDKN1C
Specificity
20 %
Genes
7 %
Short QT syndrome.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

CACNB2, CACNA1C, KCNQ1, KCNH2, KCNJ2
Specificity
40 %
Genes
13 %
Sudden Cardiac Arrest (SCA): Sequencing and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

CASQ2, KCNE2, RYR2, ANK2, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
70 %
Genes
44 %
Hearing Loss: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MASP1, MYO1A, SLC29A3, SALL4, MITF, GPSM2, MT-RNR1, RPS6KA3, GRXCR2, SYNE4, ELMOD3, TMEM132E, OTOGL, CEACAM16, POLR1D, TPRN, GRXCR1, LOXHD1, TSPEAR, TRIOBP , (...)

View the complete list with 111 more genes
Specificity
2 %
Genes
13 %
Hearing Loss: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MASP1, MYO1A, SLC29A3, SALL4, GPSM2, RPS6KA3, CEACAM16, TPRN, GRXCR1, LOXHD1, TRIOBP, TMIE, TJP2, SLC26A5, OTOA, MYH9, MYH14, LHFPL5, LRTOMT, GJB3 , (...)

View the complete list with 71 more genes
Specificity
3 %
Genes
13 %
Hearing Loss NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MYO1F, MYO1C, TMPRSS5, TBL1X, GSTP1, TCF21, MTAP, SPINK5, MYO1A, GJA1, LHX3, MITF, CATSPER2, GPSM2, TPRN, GRXCR1, LOXHD1, TRIOBP, TMIE, TJP2 , (...)

View the complete list with 83 more genes
Specificity
2 %
Genes
13 %
Short QT NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

CACNA1C, KCNQ1, KCNH2, KCNJ2
Specificity
50 %
Genes
13 %
Nuclear-Mito NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

CNR1, CHDH, CLYBL, NIPSNAP3A, IDE, IMMT, LETM1, MAVS, RAB11FIP5, POLRMT, PTGES2, PPARGC1A, AS3MT, ACSM3, ACSL5, DMAC2, ATP10D, NDUFB1, HK2, ECI1 , (...)

View the complete list with 484 more genes
Specificity
2 %
Genes
38 %
Jervell and Lange-Nielsen Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

KCNQ1, KCNE1
Specificity
100 %
Genes
13 %
Short QT Syndrome (SQTS) Panel.

By Blueprint Genetics in Finland.

CACNB2, CACNA1C, KCNQ1, KCNH2, KCNJ2
Specificity
40 %
Genes
13 %
Long QT Syndrome (LQTS) Panel.

By Blueprint Genetics in Finland.

TECRL, CALM3, NOS1AP, AKAP9, KCNJ5, KCNE2, CALM2, CALM1, ANK2, CACNA1C, KCNQ1, KCNE1, SCN5A, KCNH2, KCNJ2, CAV3
Specificity
75 %
Genes
75 %
Comprehensive Hearing Loss and Deafness Panel.

By Blueprint Genetics in Finland.

WBP2, FDXR, RMND1, CEP78, SLC52A3, SLC52A2, LRP2, MGP, SLC29A3, DCAF17, GJA1, SALL4, MITF, GPSM2, RPS6KA3, PEX26, GRXCR2, SYNE4, ELMOD3, TMEM132E , (...)

View the complete list with 159 more genes
Specificity
2 %
Genes
13 %
Syndromic Hearing Loss Panel.

By Blueprint Genetics in Finland.

FDXR, SLC52A3, SLC52A2, LRP2, MGP, DCAF17, GJA1, MITF, PEX26, POLR1D, TFAP2A, SEMA3E, PEX6, MYH9, GATA3, FOXI1, FGF3, CHSY1, SLITRK6, SIX1 , (...)

View the complete list with 66 more genes
Specificity
3 %
Genes
13 %
Arrhythmia Panel.

By Blueprint Genetics in Finland.

PPA2, CDH2, TECRL, MYL4, TNNI3K, CALM3, CTNNA3, SCN10A, NUP155, GATA6, DBH, TBX5, SALL4, NOS1AP, DSC2, TNNT2, JUP, DSG2, PLN, MYH6 , (...)

View the complete list with 35 more genes
Specificity
26 %
Genes
88 %
Comprehensive Cardiology Panel.

By Blueprint Genetics in Finland.

PLEKHM2, PPA2, LRRC10, FBXO32, MYBPHL, CDH2, HAND1, FOXD4, TECRL, RMND1, GTPBP3, MYL4, TNNI3K, TAB2, CALM3, CALR3, ALPK3, TBX20, GATA5, RBCK1 , (...)

View the complete list with 165 more genes
Specificity
8 %
Genes
88 %
Long QT syndrome type I.

By Bioarray in Spain.

KCNQ1
Specificity
100 %
Genes
7 %
Short QT Syndrome Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

CACNB2, CACNA1C, KCNQ1, KCNH2, KCNJ2
Specificity
40 %
Genes
13 %
KCNQ1 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

KCNQ1
Specificity
100 %
Genes
7 %
Short QT Syndrome NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

CACNB2, CACNA1C, KCNQ1, CACNA2D1, KCNH2, KCNJ2
Specificity
34 %
Genes
13 %
Long QT Syndrome 1 (KCNQ1) Targeted Testing.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

KCNQ1
Specificity
100 %
Genes
7 %
KCNQ1 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

KCNQ1
Specificity
100 %
Genes
7 %
Otogenetics Hearing Loss and Deafness Multi-Gene NGS Panel.

By Otogenetics in United States.

MIR183, TFCP2, MIR182, OTOR, MYO1F, MYO1C, TMPRSS5, TBL1X, GSTP1, TCF21, HAL, ECE1, MTAP, GJB4, SPINK5, FAS, MT-TL2, MT-TM, MT-TD, MT-TQ , (...)

View the complete list with 109 more genes
Specificity
2 %
Genes
13 %
Short QT Syndrome Type 2 , Sequencing KCNQ1 Gene.

By Reference Laboratory Genetics in Spain.

KCNQ1
Specificity
100 %
Genes
7 %
Long QT Syndrome Type 1 , Sequencing KCNQ1 Gene.

By Reference Laboratory Genetics in Spain.

KCNQ1
Specificity
100 %
Genes
7 %
Short QT Syndrome , Panel Massive Sequencing (NGS) 3 Genes.

By Reference Laboratory Genetics in Spain.

KCNQ1, KCNH2, KCNJ2
Specificity
67 %
Genes
13 %
Tempus xO assay.

By Tempus Labs, Inc. in United States.

SETD6, PIM3, MAP3K10, PDGFA, MAP3K11, PAK2, KHSRP, WASL, CASC11, GLIS1, NRG2, SOX21, SMARCC1, CUL4A, UTY, WNT9A, TEF, CHIC1, TRIM28, CDK11B , (...)

View the complete list with 1693 more genes
Specificity
1 %
Genes
32 %
OtoSCOPE.

By Molecular Otolaryngology and Renal Research Laboratories University of Iowa Hospital and Clinics in United States.

LOXL3, KITLG, CRYL1, MITF, CATSPER2, GPSM2, MT-RNR1, GRXCR2, SYNE4, ELMOD3, TMEM132E, EPS8L2, OTOGL, CEACAM16, DIAPH3, POLR1D, TPRN, GRXCR1, LOXHD1, TSPEAR , (...)

View the complete list with 132 more genes
Specificity
2 %
Genes
13 %
Atrial Fibrillation Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

GJA5, NPPA, NUP155, KCNA5, KCNE2, SCN3B, SCN2B, ABCC9, KCNQ1, KCNE1, SCN5A, SCN1B, KCNH2, KCND3, KCNJ2, LMNA
Specificity
32 %
Genes
32 %
Short QT Syndrome Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

CACNB2, CACNA1C, KCNQ1, CACNA2D1, KCNH2, KCNJ2
Specificity
34 %
Genes
13 %
Beckwith-Wiedemann Syndrome.

By Genetics Laboratory Shodair Children's Hospital in United States.

H19, KCNQ1
Specificity
50 %
Genes
7 %
Cardiac Arrhythmia Gene Panel.

By Molecular Genetics Laboratory - Diagnostics Genetics LabPLUS - Auckland City Hospital in New Zealand.

SCN10A, MYL2, DSC2, RBM20, TNNT2, TPM1, DSG2, MYH6, TNNI3, KCNA5, CASQ2, KCNE2, RYR2, PKP2, CACNB2, CACNA1C, KCNQ1, KCNE1, SCN5A, SCN1B , (...)

View the complete list with 8 more genes
Specificity
22 %
Genes
38 %
KCNQ1.

By Institute for Human Genetics University Clinic Freiburg in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
KCNQ1.

By Institute for Human Genetics University Clinic Freiburg in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
OtoGenome Test for Hearing Loss (110 Genes).

By Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine) in United States.

CEP78, SLC52A3, SLC52A2, KITLG, MITF, CATSPER2, GPSM2, MT-RNR1, SYNE4, OTOGL, CEACAM16, TPRN, GRXCR1, LOXHD1, TRIOBP, TMIE, S1PR2, POU4F3, OTOA, MYH9 , (...)

View the complete list with 90 more genes
Specificity
2 %
Genes
13 %
Short QT Syndrome Sequencing Panel.

By GeneDx in United States.

KCNQ1, KCNH2, KCNJ2
Specificity
67 %
Genes
13 %
KCNQ1 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

KCNQ1
Specificity
100 %
Genes
7 %
KCNH2, KCNJ2, KCNQ1. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

KCNQ1, KCNH2, KCNJ2
Specificity
67 %
Genes
13 %
CAV3, KCNE1, KCNE2, KCNH2, KCNQ1, SCN5A. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

KCNE2, KCNQ1, KCNE1, SCN5A, KCNH2, CAV3
Specificity
100 %
Genes
38 %
KCNQ1. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

KCNQ1
Specificity
100 %
Genes
7 %
Long QT Syndrome 1 (sequence analysis of KCNQ1 gene).

By CGC Genetics in Portugal.

KCNQ1
Specificity
100 %
Genes
7 %
Syndromic deafness (NGS panel for 62 genes).

By CGC Genetics in Portugal.

MITF, POLR1D, TFAP2A, SEMA3E, GATA3, FOXI1, FGF3, CHSY1, SLITRK6, SIX1, KCNQ1, KCNE1, TCOF1, SLC19A2, SOX10, SNAI2, SIX5, EDNRB, PAX3, NLRP3 , (...)

View the complete list with 42 more genes
Specificity
4 %
Genes
13 %
Short QT syndrome (NGS panel for 3 genes).

By CGC Genetics in Portugal.

KCNQ1, KCNH2, KCNJ2
Specificity
67 %
Genes
13 %
Long QT syndrome 1 (LQT1, deletion/duplication analysis on KCNQ1 gene).

By CGC Genetics in Portugal.

KCNQ1
Specificity
100 %
Genes
7 %
Syndromic and non syndromic deafness (NGS panel for 127 genes).

By CGC Genetics in Portugal.

TMC2, MYO1A, MITF, GPSM2, OTOGL, CEACAM16, DIAPH3, POLR1D, TPRN, GRXCR1, LOXHD1, TSPEAR, TRIOBP, TMIE, TFAP2A, TJP2, SLC26A5, SEMA3E, POU4F3, OTOA , (...)

View the complete list with 107 more genes
Specificity
2 %
Genes
13 %
Short QT syndrome (NGS panel for 5 genes).

By CGC Genetics in Portugal.

CACNB2, CACNA1C, KCNQ1, KCNH2, KCNJ2
Specificity
40 %
Genes
13 %
Jervell and Lange-Nielsen syndrome (sequence analysis of KCNQ1 gene).

By CGC Genetics in Portugal.

KCNQ1
Specificity
100 %
Genes
7 %
Jervell and Lange-Nielsen syndrome (NGS panel of 2 genes).

By CGC Genetics in Portugal.

KCNQ1, KCNE1
Specificity
100 %
Genes
13 %
Long QT Syndrome and Jervell and Lange-Nielsen syndrome via the KCNQ1 Gene.

By PreventionGenetics PreventionGenetics in United States.

KCNQ1
Specificity
100 %
Genes
7 %
Short QT Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

CACNB2, CACNA1C, KCNQ1, CACNA2D1, KCNH2, KCNJ2
Specificity
34 %
Genes
13 %
Short QT syndrome Comprehensive panel.

By Connective Tissue Gene Tests in United States.

CACNB2, CACNA1C, KCNQ1, CACNA2D1, KCNH2, KCNJ2
Specificity
34 %
Genes
13 %
Short QT syndrome Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

CACNB2, CACNA1C, KCNQ1, CACNA2D1, KCNH2, KCNJ2
Specificity
34 %
Genes
13 %
Short QT syndrome NGS panel.

By Connective Tissue Gene Tests in United States.

CACNB2, CACNA1C, KCNQ1, CACNA2D1, KCNH2, KCNJ2
Specificity
34 %
Genes
13 %
Short QT syndrome.

By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München in Germany.

KCNQ1, KCNH2
Specificity
100 %
Genes
13 %
Jervell and Lange-Nielsen syndrome type 1.

By Centogene AG - the Rare Disease Company in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
Atrial fibrillation type 3.

By Centogene AG - the Rare Disease Company in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
Long QT syndrome.

By bio.logis Center for Human Genetics Diagnosticum in Germany.

KCNQ1, KCNH2
Specificity
100 %
Genes
13 %
QT syndrome, KCNQ1.

By GGA - Galil Genetic Analysis in Israel.

KCNQ1
Specificity
100 %
Genes
7 %
KCNQ1-Related Familial Atrial Fibrillation.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
Long QT Syndrome 1.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
Long QT Syndrome (KCNQ1, KCNH2, KCNE1;MLPA).

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

KCNQ1, KCNE1, KCNH2
Specificity
100 %
Genes
19 %
Standard Long QT syndrome Stage 1.

By Health in Code in Spain.

KCNE2, KCNQ1, KCNE1, SCN5A, KCNH2
Specificity
100 %
Genes
32 %
Standard Short QT syndrome.

By Health in Code in Spain.

KCNQ1, KCNH2, KCNJ2
Specificity
67 %
Genes
13 %
Short QT Syndrome Panel.

By Health in Code in Spain.

CACNB2, CACNA1C, KCNQ1, CACNA1D, CACNA2D1, KCNH2, KCNJ2
Specificity
29 %
Genes
13 %
Cardiomyopathies General Panel.

By Health in Code in Spain.

NNT, MYOM1, PPP1R13L, PERP, FHOD3, FOXD4, MRPL44, COA6, TRIM63, KLF10, PKP4, TNNI3K, CALR3, MIB1, TBX20, CAVIN4, CHRM2, GATA5, CTNNA3, COA5 , (...)

View the complete list with 153 more genes
Specificity
3 %
Genes
32 %
Long QT syndrome type 1: KCNQ1 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KCNQ1
Specificity
100 %
Genes
7 %
KCNQ1.

By Fulgent Genetics Fulgent Genetics in United States.

KCNQ1
Specificity
100 %
Genes
7 %
Atrial Fibrillation Panel.

By Blueprint Genetics in Finland.

SCN10A, NUP155, GATA6, TBX5, KCNA5, KCNJ5, KCNE2, RYR2, CACNB2, SCN3B, KCNQ1, KCNE1, SCN5A, HCN4, SCN1B, KCNH2, KCNJ2, LDB3, LMNA
Specificity
37 %
Genes
44 %
Long QT syndrome type I.

By Bioarray in Spain.

KCNQ1
Specificity
100 %
Genes
7 %
iGene Cardiac Panel.

By ApolloGen, Inc. in United States.

APOB, PCSK9, MYL3, TNNT2, TPM1, DSG2, PRKAG2, TNNI3, ACTC1, RYR2, PKP2, KCNQ1, SCN5A, KCNH2, MYBPC3, MYH7, TTN, LMNA, LDLR, GLA , (...)

View the complete list with 2 more genes
Specificity
14 %
Genes
19 %
Short QT Syndrome Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

CACNB2, CACNA1C, KCNQ1, CACNA2D1, KCNH2, KCNJ2
Specificity
34 %
Genes
13 %
LONG QT SYNDROME, JERVELL AND LANGE-NIELSEN SYNDROME (AUTOSOMAL RECESSIVE).

By Laboratorio de Genetica Clinica SL in Spain.

KCNQ1, KCNE1
Specificity
100 %
Genes
13 %
LONG QT SYNDROME, ROMANO-WARD SYNDROME.

By Laboratorio de Genetica Clinica SL in Spain.

KCNE2, KCNQ1, KCNE1, SCN5A, KCNH2
Specificity
100 %
Genes
32 %
BRUGADA SYNDROME/LONG-QT/SHORT-QT/VENTRICULAR TACHYCARDIA: NGS PANEL.

By Laboratorio de Genetica Clinica SL in Spain.

AKAP9, CASQ2, SNTA1, KCNE2, TRDN, CALM2, CALM1, RYR2, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, TRPM4, CACNA1C, KCNQ1, KCNE1, SCN5A , (...)

View the complete list with 5 more genes
Specificity
44 %
Genes
69 %
Long QT Syndrome , Deletions-Duplications (MLPA) KCNQ1,KCNH2,KCNE1,KCNE2 Genes.

By Reference Laboratory Genetics in Spain.

KCNE2, KCNQ1, KCNE1, KCNH2
Specificity
100 %
Genes
25 %
Long QT syndrome 1.

By Labor Dr. Wisplinghoff in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
Jervell and Lange-Nielsen syndrome 1.

By Labor Dr. Wisplinghoff in Germany.

KCNQ1
Specificity
100 %
Genes
7 %
Phosphorus Short QT Syndrome Panel.

By Phosphorus Diagnostics LLC in United States.

CACNB2, CACNA1C, KCNQ1, CACNA2D1, KCNH2, KCNJ2
Specificity
34 %
Genes
13 %
Jervell and Lange-Nielsen Syndrome: gene sequencing.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

KCNQ1, KCNE1
Specificity
100 %
Genes
13 %
KCNE1.

By Institute for Human Genetics University Clinic Freiburg in Germany.

KCNE1
Specificity
100 %
Genes
7 %
KCNE1 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

KCNE1
Specificity
100 %
Genes
7 %
Long QT syndrome 1, LQT5 (deletion/duplication analysis of KCNE1 gene).

By CGC Genetics in Portugal.

KCNE1
Specificity
100 %
Genes
7 %
Long QT syndrome 5 (LQT5, sequence analysis of KCNE1 gene).

By CGC Genetics in Portugal.

KCNE1
Specificity
100 %
Genes
7 %
Jervell and Lange-Nielsen syndrome type 2.

By Centogene AG - the Rare Disease Company in Germany.

KCNE1
Specificity
100 %
Genes
7 %
Long QT Syndrome 5.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

KCNE1
Specificity
100 %
Genes
7 %
Jervell and Lange-Nielsen syndrome 2.

By Praxis fuer Humangenetik Wien in Austria.

KCNE1
Specificity
100 %
Genes
7 %
Jervell and Lange-Nielsen syndrome 2.

By MedGene in Slovakia.

KCNE1
Specificity
100 %
Genes
7 %
Long QT syndrome type 5 and 6: KCNE1 and KCNE2 genes sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KCNE2, KCNE1
Specificity
100 %
Genes
13 %
Long QT syndrome type 5: KCNE1 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KCNE1
Specificity
100 %
Genes
7 %
Long QT syndrome type V.

By Bioarray in Spain.

KCNE1
Specificity
100 %
Genes
7 %
KCNE1.

By Institute for Human Genetics University Clinic Freiburg in Germany.

KCNE1
Specificity
100 %
Genes
7 %
KCNE1. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

KCNE1
Specificity
100 %
Genes
7 %
Jervell and Lange-Nielsen syndrome (sequence analysis of KCNE1 gene).

By CGC Genetics in Portugal.

KCNE1
Specificity
100 %
Genes
7 %
Long QT Syndrome and Jervell and Lange-Nielsen Syndrome via the KCNE1 Gene.

By PreventionGenetics PreventionGenetics in United States.

KCNE1
Specificity
100 %
Genes
7 %
Long QT syndrome type 5.

By Centogene AG - the Rare Disease Company in Germany.

KCNE1
Specificity
100 %
Genes
7 %
Single gene testing KCNE1.

By CeGaT GmbH in Germany.

KCNE1
Specificity
100 %
Genes
7 %
Long QT Syndrome 5.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

KCNE1
Specificity
100 %
Genes
7 %
KCNE1 gene sequencing.

By Health in Code in Spain.

KCNE1
Specificity
100 %
Genes
7 %
Long QT syndrome 5.

By Praxis fuer Humangenetik Wien in Austria.

KCNE1
Specificity
100 %
Genes
7 %
Long QT syndrome 5.

By MedGene in Slovakia.

KCNE1
Specificity
100 %
Genes
7 %
KCNE1.

By Fulgent Genetics Fulgent Genetics in United States.

KCNE1
Specificity
100 %
Genes
7 %
Long QT syndrome type V.

By Bioarray in Spain.

KCNE1
Specificity
100 %
Genes
7 %
KCNE1 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

KCNE1
Specificity
100 %
Genes
7 %
KCNE1 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

KCNE1
Specificity
100 %
Genes
7 %
Long QT Syndrome Type 5 , Sequencing KCNE1 Gene.

By Reference Laboratory Genetics in Spain.

KCNE1
Specificity
100 %
Genes
7 %
Long QT syndrome 5.

By Labor Dr. Wisplinghoff in Germany.

KCNE1
Specificity
100 %
Genes
7 %
Jervell and Lange-Nielsen syndrome 2.

By Labor Dr. Wisplinghoff in Germany.

KCNE1
Specificity
100 %
Genes
7 %
Epilepsy Advanced Sequencing and CNV Evaluation - Generalized, Absence, Focal,Febrile and Myoclonic Epilepsies.

By Athena Diagnostics Inc in United States.

BCKDK, PIGO, BRAT1, PRRT2, DEPDC5, PRIMA1, TBC1D24, ASAH1, ALG13, SLC4A10, SCN5A, SCARB2, KCNMA1, MBD5, LMNB2, HCN4, GRIN2A, GABRG2, GABRA1, EPM2A , (...)

View the complete list with 64 more genes
Specificity
3 %
Genes
13 %
Epilepsy Advanced Sequencing and CNV Evaluation.

By Athena Diagnostics Inc in United States.

IQSEC2, ATRX, SMS, OFD1, SERPINI1, KIF1BP, CNTNAP2, RNASEH2B, RNASEH2C, RNASEH2A, TCF4, KCNJ10, SAMHD1, PNKP, SPTAN1, PLCB1, ANKRD11, PIGV, PIGN, DYRK1A , (...)

View the complete list with 214 more genes
Specificity
1 %
Genes
13 %
NGS Epilepsy/Seizure Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

ATR, PCNT, FLVCR2, CDK5RAP2, GLI2, CDON, FOXH1, NODAL, ABCB1, CEP152, NALCN, ZIC2, TGIF1, TUBB2A, TSEN2, TSEN34, EXOSC3, KCNAB1, VANGL1, MTOR , (...)

View the complete list with 125 more genes
Specificity
1 %
Genes
7 %
Dilated & Arrhythmogenic Cardiomyopathies Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6, TNNI3 , (...)

View the complete list with 31 more genes
Specificity
4 %
Genes
13 %
Brugada Syndrome.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

GPD1L, CACNB2, KCNE3, SCN3B, TRPM4, CACNA1C, SCN5A, HCN4, SCN1B
Specificity
12 %
Genes
7 %
Atrioventricular Block Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

NKX2-5, TRPM4, SCN5A, SCN1B, EMD, DES, LMNA
Specificity
15 %
Genes
7 %
Dilated Cardiomyopathy Panel (30 genes).

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

VCL, CSRP3, ACTN2, RBM20, TNNT2, TPM1, MYPN, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, ACTC1, NEBL, ABCC9, LAMP2, SCN5A, SGCD, TCAP , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
7 %
DCM and DMD related Cardiomyopathy.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

VCL, CSRP3, ACTN2, RBM20, TNNT2, TPM1, MYPN, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, ACTC1, NEBL, ABCC9, LAMP2, SCN5A, SGCD, TCAP , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
7 %
SCN5A.

By Institute for Human Genetics University Clinic Freiburg in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Brugada Syndrome Sequencing Panel.

By GeneDx in United States.

GPD1L, CACNB2, KCNE3, SCN3B, CACNA1C, SCN5A, SCN1B
Specificity
15 %
Genes
7 %
Comprehensive Cardiomyopathy Panel.

By GeneDx in United States.

MT-TL2, MT-TM, MT-TD, MT-TQ, MT-TH, MT-TI, MT-TG, TMPO, MT-ND5, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1 , (...)

View the complete list with 56 more genes
Specificity
3 %
Genes
13 %
DCM/LVNC Sequencing Panel.

By GeneDx in United States.

MT-TL2, MT-TM, MT-TD, MT-TQ, MT-TH, MT-TI, MT-ND5, VCL, CSRP3, ACTN2, RBM20, TNNT2, TPM1, NEXN, PLN, TNNI3, TNNC1, ANKRD1, ACTC1, LAMP2 , (...)

View the complete list with 17 more genes
Specificity
3 %
Genes
7 %
DCMNext with TTN.

By Ambry Genetics in United States.

TBX20, TMPO, TXNRD2, VCL, CSRP3, ACTN2, RBM20, TNNT2, TPM1, MYPN, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, NKX2-5, LAMA4, ACTC1, ABCC9 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
7 %
SCN5A mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

SCN5A
Specificity
100 %
Genes
7 %
LMNA, MYBPC3, MYH7, SCN5A, TNNI3, TNNT2. NextGeneDx.Complete sequencing by NGS.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

TNNT2, TNNI3, SCN5A, MYBPC3, MYH7, LMNA
Specificity
17 %
Genes
7 %
SCN5A. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

SCN5A
Specificity
100 %
Genes
7 %
SCN5A-Related Dilated Cardiomyopathy.

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
7 %
Long QT syndrome 3 (sequence analysis of SCN5A gene).

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
7 %
Brugada Syndrome 1 (sequence analysis of SCN5A gene).

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
7 %
Brugada syndrome (NGS panel for 7 genes).

By CGC Genetics in Portugal.

GPD1L, CACNB2, KCNE3, SCN3B, CACNA1C, SCN5A, SCN1B
Specificity
15 %
Genes
7 %
Sinus node syndrome (NGS panel for 3 genes).

By CGC Genetics in Portugal.

MYH6, SCN5A, HCN4
Specificity
34 %
Genes
7 %
Familial dilated cardiomyopathy type 1E (deletions/duplications analysis of SCN5A gene).

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
7 %
Brugada Syndrome type 1.

By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine in United States.

SCN5A
Specificity
100 %
Genes
7 %
Brugada Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

KCNE5, RANGRF, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, KCNJ8, SLMAP, TRPM4, CACNA1C, CACNA2D1, SCN5A, HCN4, SCN1B, KCND3
Specificity
7 %
Genes
7 %
Epilepsy and Seizure Plus Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

DENND5A, RBFOX3, HECW2, GUF1, KPNA7, STRADA, RAB11A, NUS1, ITPA, CNTN2, SNX27, ARHGEF15, PPP3CA, PIK3AP1, JMJD1C, AP3B2, FASN, YWHAG, KCND2, RYR3 , (...)

View the complete list with 202 more genes
Specificity
1 %
Genes
13 %
Atrioventricular block Deletion/ Duplication panel.

By Connective Tissue Gene Tests in United States.

NKX2-5, TRPM4, SCN5A, SCN1B, EMD, DES, LMNA
Specificity
15 %
Genes
7 %
Brugada syndrome and related disorders Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

KCND2, KCNE5, SCN10A, FGF12, SEMA3A, RANGRF, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, ABCC9, KCNJ8, SLMAP, CACNA1C, CACNA2D1, SCN5A, HCN4 , (...)

View the complete list with 6 more genes
Specificity
20 %
Genes
32 %
Brugada syndrome and related disorders NGS panel.

By Connective Tissue Gene Tests in United States.

KCND2, KCNE5, SCN10A, FGF12, SEMA3A, RANGRF, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, ABCC9, KCNJ8, SLMAP, CACNA1C, CACNA2D1, SCN5A, HCN4 , (...)

View the complete list with 6 more genes
Specificity
20 %
Genes
32 %
Brugada syndrome and related disorders Comprehensive panel.

By Connective Tissue Gene Tests in United States.

KCND2, KCNE5, SCN10A, FGF12, SEMA3A, RANGRF, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, ABCC9, KCNJ8, SLMAP, CACNA1C, CACNA2D1, SCN5A, HCN4 , (...)

View the complete list with 6 more genes
Specificity
20 %
Genes
32 %
Progressive familial heart block type I NGS panel.

By Connective Tissue Gene Tests in United States.

TRPM4, SCN5A
Specificity
50 %
Genes
7 %
Progressive familial heart block type I Comprehensive panel.

By Connective Tissue Gene Tests in United States.

TRPM4, SCN5A
Specificity
50 %
Genes
7 %
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) / Arrhythmogenic Right Ventricular Dysplasia (ARVD).

By MGZ Medical Genetics Center in Germany.

CASQ2, CALM1, SCN5A
Specificity
67 %
Genes
13 %
Dilated Cardiomyopathy Sequential Panel.

By FirmaLab in United States.

TNNT2, ACTC1, SCN5A, MYH7, TTN, LMNA
Specificity
17 %
Genes
7 %
Brugada Syndrome 1.

By Bioscientia GmbH Center for Human Genetics in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Brugada syndrome.

By Synlab MVZ Humane Genetik München Synlab MVZ Humane Genetik München in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Cardiomyopathy panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

MYOZ1, TRIM63, CALR3, TMPO, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2 , (...)

View the complete list with 41 more genes
Specificity
4 %
Genes
13 %
Ventricular fibrillation, paroxysmal familial type 1.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Brugada syndrome panel.

By Centogene AG - the Rare Disease Company in Germany.

GPD1L, CACNB2, KCNE3, SCN3B, SLMAP, CACNA1C, SCN5A, HCN4, SCN1B
Specificity
12 %
Genes
7 %
Atrial fibrillation type 10.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Cardiomyopathy, dilated type 1E.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Heart block type 1.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
7 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company in Germany.

FCGR2B, TNF, ALOX5AP, PRKCH, TLR5, TIRAP, NOS2, XBP1, KCNK18, AANAT, SNIP1, EIF4E, ZBTB18, ADAM10, YAP1, ICAM1, SNX3, CISH, TAS2R38, FRG1 , (...)

View the complete list with 1185 more genes
Specificity
1 %
Genes
19 %
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT), Paroxysmal/ Idiopathic Ventricular Fibrillation / Tachycardia Panel.

By CeGaT GmbH in Germany.

GNAI2, DPP6, CASQ2, TRDN, CALM2, CALM1, RYR2, ANK2, SCN5A, KCNJ2
Specificity
50 %
Genes
32 %
BRUGADA SYNDROME 1; BRGDA1.

By Duzen Laboratuvarlar Grubu Biyolojik Bilimler Arastirma Gelistirme ve Uretim AS in Turkey.

SCN5A
Specificity
100 %
Genes
7 %
SCN5A sequencing.

By DNAbiolab Cretan Center for Research and Development of Applications on Genetics and Molecular Biology in Greece.

SCN5A
Specificity
100 %
Genes
7 %
QT syndrome, SCN5A.

By GGA - Galil Genetic Analysis in Israel.

SCN5A
Specificity
100 %
Genes
7 %
Dilated Cardiomyopathy.

By Asper Biogene Asper Biogene LLC in Estonia.

TBX20, TMPO, VCL, DSC2, CSRP3, ACTN2, RBM20, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, LAMA4 , (...)

View the complete list with 22 more genes
Specificity
3 %
Genes
7 %
Dilated cardiomyopathy with conduction disorders Stage 3.

By Health in Code in Spain.

SCN5A
Specificity
100 %
Genes
7 %
J Wave Syndrome Panel.

By Health in Code in Spain.

KCNE5, SCN10A, ANK3, RANGRF, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, ABCC9, KCNJ8, SLMAP, TRPM4, CACNA1C, CACNA1D, CACNA2D1, SCN5A, HCN4 , (...)

View the complete list with 3 more genes
Specificity
18 %
Genes
25 %
Brugada Syndrome Panel.

By Health in Code in Spain.

KCNE5, SCN10A, ANK3, RANGRF, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, ABCC9, KCNJ8, SLMAP, TRPM4, CACNA1C, CACNA1D, CACNA2D1, SCN5A, HCN4 , (...)

View the complete list with 3 more genes
Specificity
18 %
Genes
25 %
SCN5A-Related Disorders.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

SCN5A
Specificity
100 %
Genes
7 %
Long QT Syndrome 3.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

SCN5A
Specificity
100 %
Genes
7 %
Invitae Dilated Cardiomyopathy Panel.

By Invitae in United States.

VCL, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, TNNI3, TNNC1, ACTC1, RYR2, PKP2, ABCC9, LAMP2, SCN5A, SGCD, TCAP , (...)

View the complete list with 21 more genes
Specificity
5 %
Genes
13 %
Invitae Left Ventricular Noncompaction Panel.

By Invitae in United States.

VCL, TNNT2, TPM1, PLN, TNNI3, ACTC1, RYR2, LAMP2, SCN5A, HCN4, MYBPC3, MYH7, LMNA, TAZ, DSP
Specificity
7 %
Genes
7 %
Invitae Cardiomyopathy and Skeletal Muscle Disease Panel.

By Invitae in United States.

STIM1, VCL, GMPPB, LMOD3, STAC3, POMK, TNPO3, KLHL41, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, MYPN, JUP, DSG2, PLN , (...)

View the complete list with 93 more genes
Specificity
2 %
Genes
13 %
Invitae Brugada Syndrome Panel.

By Invitae in United States.

PKP2, GPD1L, CACNB2, ABCC9, CACNA1C, SCN5A, HCN4, KCNH2
Specificity
25 %
Genes
13 %
Dilated cardiomyopathy: SCN5A gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

SCN5A
Specificity
100 %
Genes
7 %
CARDIOMYOPATHY, DILATED (DCM.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

TMPO, VCL, CSRP3, ACTN2, RBM20, TNNT2, TPM1, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, ACTC1, LAMP2, SCN5A, SGCD, TCAP, MYBPC3 , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
7 %
Catecholaminergic Polymorphic Ventricular Tachycardia.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

CASQ2, TRDN, CALM1, RYR2, ANK2, SCN5A, KCNJ2
Specificity
58 %
Genes
25 %
Dilated Cardiomyopathy: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

VCL, CSRP3, ACTN2, RBM20, GATAD1, TNNT2, TPM1, MYPN, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, PRDM16, LAMA4, ACTC1, NEBL, PDLIM3 , (...)

View the complete list with 19 more genes
Specificity
3 %
Genes
7 %
Brugada Syndrome: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

GPD1L, CACNB2, KCNE3, SCN3B, CACNA1C, SCN5A, HCN4, SCN1B
Specificity
13 %
Genes
7 %
Cardiomyopathy: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6 , (...)

View the complete list with 45 more genes
Specificity
4 %
Genes
13 %
Dilated Cardiomyopathy: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

VCL, CSRP3, ACTN2, RBM20, GATAD1, TNNT2, TPM1, MYPN, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, LAMA4, ACTC1, NEBL, ABCC9, LAMP2 , (...)

View the complete list with 17 more genes
Specificity
3 %
Genes
7 %
Familial Cardiomyopathy Full Gene Sequencing Panel.

By Integrated Genetics Westborough Integrated Genetics in United States.

HOPX, APOA1, TMPO, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, MYH6, TNNI3, TNNC1 , (...)

View the complete list with 26 more genes
Specificity
5 %
Genes
13 %
Brugada Syndrome Panel.

By Blueprint Genetics in Finland.

CACNB2, SCN3B, TRPM4, CACNA1C, SCN5A, HCN4, SCN1B, KCNH2, CAV3
Specificity
34 %
Genes
19 %
Brugada syndrome type I.

By Bioarray in Spain.

SCN5A
Specificity
100 %
Genes
7 %
Cardiomyopathy, dilated type 1E.

By Bioarray in Spain.

SCN5A
Specificity
100 %
Genes
7 %
Long QT syndrome type III.

By Bioarray in Spain.

SCN5A
Specificity
100 %
Genes
7 %
Dilated Cardiomyopathy Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

TMPO, FHL2, CTF1, VCL, CSRP3, ACTN2, RBM20, GATAD1, TNNT2, TPM1, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, ACTC1, ABCC9, LAMP2, SCN5A , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
7 %
Comprehensive Cardiomyopathy Panel.

By ApolloGen, Inc. in United States.

MT-TL2, MT-TM, MT-TD, MT-TQ, MT-TH, MT-TI, MT-TG, TMPO, VCL, MYL3, MYL2, ACTN2, RBM20, TNNT2, TPM1, MYPN, PLN, PRKAG2, MYH6, TNNI3 , (...)

View the complete list with 24 more genes
Specificity
5 %
Genes
13 %
Brugada Syndrome Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

SCN5A
Specificity
100 %
Genes
7 %
Familial Dilated Cardiomyopathy Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

VCL, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, ACTC1, PKP2, ABCC9, LAMP2 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
7 %
Left Ventricular Noncompaction Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

VCL, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, ACTC1, PKP2, ABCC9, LAMP2 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
7 %
Arrhythmogenic Right Ventricular Cardiomyopathy Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

DSC2, JUP, DSG2, PLN, TGFB3, RYR2, PKP2, SCN5A, TMEM43, DES, TTN, LMNA, DSP
Specificity
8 %
Genes
7 %
BRUGADA SYNDROME.

By Laboratorio de Genetica Clinica SL in Spain.

GPD1L, CACNB2, KCNE3, SCN3B, TRPM4, CACNA1C, SCN5A, HCN4, SCN1B
Specificity
12 %
Genes
7 %
Long QT Syndrome Type 3 , Sequencing SCN5A Gene.

By Reference Laboratory Genetics in Spain.

SCN5A
Specificity
100 %
Genes
7 %
Dilated Cardiomyopathy, Sequencing SCN5A Gene.

By Reference Laboratory Genetics in Spain.

SCN5A
Specificity
100 %
Genes
7 %
Dilated Cardiomyopathy, Panel Massive Sequencing (NGS) 30 Genes.

By Reference Laboratory Genetics in Spain.

VCL, CSRP3, ACTN2, RBM20, TNNT2, TPM1, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ACTC1, LAMP2, SCN5A, SGCD, TCAP, MYBPC3, BAG3, LDB3 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
7 %
Brugada Syndrome, Panel Massive Sequencing (NGS) 8 Genes.

By Reference Laboratory Genetics in Spain.

GPD1L, CACNB2, KCNE3, SCN3B, CACNA1C, SCN5A, HCN4, SCN1B
Specificity
13 %
Genes
7 %
Cardiac Conduction System Related Disorders , Panel Massive Sequencing (NGS) 20 Genes.

By Reference Laboratory Genetics in Spain.

TNNI3K, SCN10A, GJA5, TBX5, PRKAG2, NKX2-5, ACTC1, TRPM4, LAMP2, CACNA1D, SCN5A, HCN4, SCN1B, KCNJ2, EMD, DES, LMNA, GLA, GAA, TTR
Specificity
10 %
Genes
13 %
Long QT syndrome 3.

By Labor Dr. Wisplinghoff in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Phosphorus Pan Cardiomyopathy Including Rasopathies Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, RYR2, PKP2, ABCC9 , (...)

View the complete list with 49 more genes
Specificity
3 %
Genes
13 %
Brugada Syndrome Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

PKP2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, ABCC9, KCNJ8, SLMAP, TRPM4, CACNA1C, SCN5A, HCN4, SCN1B, KCNH2, KCND3
Specificity
13 %
Genes
13 %
Dilated Cardiomyopathy Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

TMPO, TXNRD2, CTF1, VCL, CSRP3, ACTN2, RBM20, GATAD1, TNNT2, TPM1, MYPN, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, LAMA4, ACTC1 , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
7 %
Comprehensive Cardiomyopathy Panel (37 genes).

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

VCL, MYL3, MYL2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, MYPN, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, ANKRD1, ACTC1, NEBL, ABCC9, LAMP2 , (...)

View the complete list with 17 more genes
Specificity
6 %
Genes
13 %
Brugada Syndrome Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

RANGRF, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, KCNJ8, SLMAP, TRPM4, CACNA1C, CACNA2D1, SCN5A, HCN4, SCN1B, KCND3
Specificity
7 %
Genes
7 %
Targeted CM panel.

By Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS in Italy.

DSC2, TNNT2, TPM1, JUP, DSG2, NEXN, TNNI3, PKP2, SCN5A, TMEM43, MYBPC3, LDB3, MYH7, LMNA, DSP
Specificity
7 %
Genes
7 %
DCM/Arrhythmogenic Cardiomyopathy Panel (53 Genes).

By Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine) in United States.

CAVIN4, CHRM2, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN, PRKAG2 , (...)

View the complete list with 33 more genes
Specificity
4 %
Genes
13 %
Pan Cardiomyopathy Panel (62 Genes).

By Laboratory for Molecular Medicine Laboratory for Molecular Medicine (Partners HealthCare Personalized Medicine) in United States.

CAVIN4, CHRM2, FHL2, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN , (...)

View the complete list with 41 more genes
Specificity
5 %
Genes
19 %
CMNext with TTN.

By Ambry Genetics in United States.

TBX20, TMPO, TXNRD2, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN , (...)

View the complete list with 35 more genes
Specificity
2 %
Genes
7 %
Cardiomyopathy NGS Multi-Gene Panel (50 genes), Sequence & CNV analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

CALR3, MIB1, ALPK3, CTNNA3, FHL2, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN , (...)

View the complete list with 31 more genes
Specificity
4 %
Genes
13 %
SCN5A. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

SCN5A
Specificity
100 %
Genes
7 %
SCN5A-Related Disorders.

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
7 %
Familial dilated cardiomyopathy type 1E (deletions/duplications analysis of SCN5A gene).

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
7 %
Dilated Cardiomyopathy Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

TMPO, FHL2, VCL, DSC2, CSRP3, ACTN2, RBM20, GATAD1, TNNT2, TPM1, MYPN, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, NKX2-5, PRDM16 , (...)

View the complete list with 27 more genes
Specificity
5 %
Genes
13 %
Pan Cardiomyopathy Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

CALR3, MIB1, CAVIN4, TMPO, FHL2, DPP6, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN , (...)

View the complete list with 62 more genes
Specificity
3 %
Genes
13 %
Brugada Syndrome 1 via the SCN5A Gene.

By PreventionGenetics PreventionGenetics in United States.

SCN5A
Specificity
100 %
Genes
7 %
Progressive familial heart block type I Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

TRPM4, SCN5A
Specificity
50 %
Genes
7 %
Brugada Syndrome.

By Molecular Genetics Laboratory BC Children's and BC Women's Hospitals in Canada.

SCN5A
Specificity
100 %
Genes
7 %
SCN5A-Related Disorders.

By Bioscientia GmbH Center for Human Genetics in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Long QT syndrome type 3.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Sick sinus syndrome.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Brugada syndrome type 1.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Sudden infant death syndrom.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Brugada Syndrome Panel.

By CeGaT GmbH in Germany.

SCN10A, GPD1L, CACNB2, KCNE3, SCN3B, KCNJ8, TRPM4, CACNA1C, CACNA2D1, SCN5A, HCN4, SCN1B, KCND3
Specificity
16 %
Genes
13 %
SCN5A-Related Disorders.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Brugada Syndrome 1.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Brugada Syndrome 1.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Long QT Syndrome 3.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Sick-Sinus-Syndrome 1.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN5A
Specificity
100 %
Genes
7 %
Brugada Syndrome.

By Asper Biogene Asper Biogene LLC in Estonia.

GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, TRPM4, CACNA1C, SCN5A, HCN4, SCN1B, KCND3
Specificity
10 %
Genes
7 %
Long QT syndrome, SCN5A sequencing.

By Molecular Diagnostics Laboratory Seoul National University Hospital in South Korea.

SCN5A
Specificity
100 %
Genes
7 %
SCN5A gene sequencing.

By Health in Code in Spain.

SCN5A
Specificity
100 %
Genes
7 %
Dilated Cardiomyopathy Panel.

By Health in Code in Spain.

FHOD3, FOXD4, TBX20, CAVIN4, GATA6, GATA4, TMPO, TXNRD2, FHL2, CTF1, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, GATAD1, TNNT2, TPM1 , (...)

View the complete list with 61 more genes
Specificity
3 %
Genes
13 %
Catecholaminergic Polymorphic VT Panel.

By Health in Code in Spain.

CASQ2, TRDN, CALM2, CALM1, RYR2, ANK2, SCN5A, KCNJ2
Specificity
63 %
Genes
32 %
Arrythmogenic Cardiomyopathy Panel.

By Health in Code in Spain.

CTNNA3, DSC2, JUP, DSG2, PLN, TGFB3, CASQ2, RYR2, PKP2, SCN5A, TMEM43, LDB3, FLNC, DES, TTN, LMNA, DSP
Specificity
6 %
Genes
7 %
Arrhythmogenic cardiomyopathy.

By Health in Code in Spain.

PPP1R13L, PERP, PKP4, CTNNA3, DSC2, JUP, DSG2, PLN, TGFB3, CASQ2, RYR2, PKP2, CTNNB1, SCN5A, TMEM43, LDB3, FLNC, DES, TTN, LMNA , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
7 %
Brugada syndrome / J wave syndrome.

By Health in Code in Spain.

KCND2, KCNE5, SCN10A, FGF12, ANK3, RANGRF, ANK2, PKP2, GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, ABCC9, KCNJ8, SLMAP, TRPM4, CACNA1C, CACNA1D, CACNA2D1 , (...)

View the complete list with 5 more genes
Specificity
16 %
Genes
25 %
Catecholaminergic polymorphic ventricular tachycardia panel.

By Health in Code in Spain.

CALM3, CASQ2, TRDN, CALM2, CALM1, RYR2, ANK2, SCN5A, KCNJ2
Specificity
56 %
Genes
32 %
Brugada Syndrome 1.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

SCN5A
Specificity
100 %
Genes
7 %
SCN5A-Related Dilated Cardiomyopathy.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

SCN5A
Specificity
100 %
Genes
7 %
SCN5A Gene Sequencing.

By GENETIX Centro de Investigación en Genética Humana y Reproductiva in Colombia.

SCN5A
Specificity
100 %
Genes
7 %
Invitae Arrhythmogenic Cardiomyopathy Panel.

By Invitae in United States.

DSC2, ACTN2, RBM20, TNNT2, JUP, DSG2, PLN, PRKAG2, TNNI3, RYR2, PKP2, SCN5A, EMD, TMEM43, FLNC, DES, TTN, LMNA, DSP
Specificity
6 %
Genes
7 %
Invitae Cardiomyopathy Comprehensive Panel.

By Invitae in United States.

VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, ACTC1, RYR2, PKP2, ABCC9, LAMP2 , (...)

View the complete list with 30 more genes
Specificity
4 %
Genes
13 %
Brugada syndrome: SCN5A gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

SCN5A
Specificity
100 %
Genes
7 %
Long QT syndrome type 3: SCN5A gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

SCN5A
Specificity
100 %
Genes
7 %
BRUGADA SYNDROME.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KCNE5, RANGRF, GPD1L, CACNB2, KCNE3, SCN3B, KCNJ8, TRPM4, CACNA1C, CACNA2D1, SCN5A, HCN4, SCN1B, KCND3
Specificity
8 %
Genes
7 %
Brugada Syndrome: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

GPD1L, CACNB2, KCNE3, SCN3B, CACNA1C, SCN5A, HCN4, SCN1B
Specificity
13 %
Genes
7 %
Cardiomyopathy: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6 , (...)

View the complete list with 42 more genes
Specificity
4 %
Genes
13 %
Brugada Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

GPD1L, CACNB2, KCNE3, SCN3B, CACNA1C, SCN5A, HCN4, SCN1B
Specificity
13 %
Genes
7 %
Hypertrophic Cardiomyopathy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

TMPO, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, JUP, DSG2, NEXN, PLN , (...)

View the complete list with 43 more genes
Specificity
4 %
Genes
13 %
SCN5A.

By Fulgent Genetics Fulgent Genetics in United States.

SCN5A
Specificity
100 %
Genes
7 %
Early-Onset Epileptic Encephalopathy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

RBFOX3, KPNA7, ARHGEF15, HCN2, TNK2, SLC12A5, ACY1, KCNH5, MTOR, NEDD4L, CLCN4, ZEB2, ATP6AP2, SYN1, ARHGEF9, IQSEC2, CNTNAP2, TCF4, KCNJ10, PNKP , (...)

View the complete list with 113 more genes
Specificity
2 %
Genes
13 %
Cardiomyopathy Panel.

By Blueprint Genetics in Finland.

PLEKHM2, PPA2, LRRC10, FBXO32, MYBPHL, CDH2, HAND1, FOXD4, RMND1, GTPBP3, MYL4, TNNI3K, TAB2, CALR3, ALPK3, TBX20, RBCK1, CTNNA3, EPG5, XK , (...)

View the complete list with 135 more genes
Specificity
1 %
Genes
7 %
Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel.

By Blueprint Genetics in Finland.

PLEKHM2, FBXO32, CTNNA3, VCL, DTNA, DSC2, RBM20, JPH2, TNNT2, TPM1, JUP, DSG2, PLN, MYH6, RYR2, PKP2, ABCC9, LAMP2, SCN5A, HCN4 , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
7 %
Dilated Cardiomyopathy (DCM) Panel.

By Blueprint Genetics in Finland.

PLEKHM2, LRRC10, FBXO32, GATAD2A, MYBPHL, HAND1, FOXD4, RMND1, MYL4, TNNI3K, TAB2, ALPK3, TBX20, RBCK1, EPG5, GATA6, APOA1, TBX5, VCL, SPEG , (...)

View the complete list with 50 more genes
Specificity
2 %
Genes
7 %
Long QT syndrome type III.

By Bioarray in Spain.

SCN5A
Specificity
100 %
Genes
7 %
Brugada Syndrome Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

PKP2, GPD1L, CACNB2, KCNE3, SCN3B, KCNJ8, CACNA1C, SCN5A, HCN4, SCN1B, KCND3
Specificity
10 %
Genes
7 %
Cardiomyopathy Gene Set.

By Genomics and Pathology Services Washington University in St. Louis in United States.

TMPO, FHL2, CTF1, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, GATAD1, TNNT2, TPM1, JUP, DSG2, NEXN, PLN, PRKAG2 , (...)

View the complete list with 39 more genes
Specificity
2 %
Genes
7 %
Brugada Syndrome Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

GPD1L, CACNB2, KCNE3, SCN3B, SCN2B, KCNJ8, TRPM4, CACNA1C, CACNA2D1, SCN5A, HCN4, SCN1B, KCND3
Specificity
8 %
Genes
7 %
SCN5A Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

SCN5A
Specificity
100 %
Genes
7 %
Dilated Cardiomyopathy Panel.

By ApolloGen, Inc. in United States.

MT-TL2, MT-TM, MT-TQ, MT-TH, MT-TI, TMPO, VCL, ACTN2, RBM20, TNNT2, TPM1, MYPN, PLN, MYH6, TNNI3, LAMA4, ACTC1, ABCC9, MT-TS2, MT-TS1 , (...)

View the complete list with 13 more genes
Specificity
4 %
Genes
7 %
Cardiomyopathy Exome Panel.

By Northwest Clinical Genomics Laboratory University of Washington in United States.

CAVIN4, CHRM2, TMPO, FHL2, VCL, DTNA, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, MYPN, JUP, DSG2, NEXN , (...)

View the complete list with 55 more genes
Specificity
4 %
Genes
19 %
SCN5A Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

SCN5A
Specificity
100 %
Genes
7 %
Channelopathies.

By Cardiovascular Genetics PO San Francesco-NUORO (IT) in Italy.

KCNQ1-AS1, CASQ2, RYR2, SCN5A, KCNH2
Specificity
40 %
Genes
13 %
FAMILIAL DILATED CARDIOMYOPATHY.

By Laboratorio de Genetica Clinica SL in Spain.

TMPO, VCL, CSRP3, ACTN2, RBM20, TNNT2, TPM1, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, ACTC1, SCN5A, TCAP, MYBPC3, BAG3, LDB3 , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
7 %
FAMILIAL DILATED CARDIOMYOPATHY/HYPERTROPHIC/NONCOMPACTION: NGS PANEL.

By Laboratorio de Genetica Clinica SL in Spain.

CALR3, MIB1, TBX20, GATA6, TBX5, VCL, DTNA, MYL3, MYL2, CSRP3, ACTN2, RBM20, MYOZ2, JPH2, GATAD1, TNNT2, TPM1, MYPN, DSG2, NEXN , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
7 %
Brugada Syndrome Type 1 , Sequencing SCN5A Gene.

By Reference Laboratory Genetics in Spain.

SCN5A
Specificity
100 %
Genes
7 %
Phosphorus Dilated Cardiomyopathy Including Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, TNNI3, TNNC1, ACTC1, RYR2, PKP2, ABCC9, LAMP2, SCN5A, SGCD, TCAP , (...)

View the complete list with 28 more genes
Specificity
5 %
Genes
13 %
Phosphorus Pan Cardiomyopathy Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, RYR2, PKP2, ABCC9 , (...)

View the complete list with 32 more genes
Specificity
4 %
Genes
13 %
Phosphorus Pan Cardiomyopathy Including Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, RYR2, PKP2, ABCC9 , (...)

View the complete list with 40 more genes
Specificity
4 %
Genes
13 %
Phosphorus Pan Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, PRKAG2, TNNI3, TNNC1, TGFB3, ACTC1, RYR2, PKP2, ABCC9 , (...)

View the complete list with 57 more genes
Specificity
3 %
Genes
13 %
Phosphorus Brugada Syndrome Panel.

By Phosphorus Diagnostics LLC in United States.

SCN10A, PKP2, GPD1L, CACNB2, KCNE3, ABCC9, CACNA1C, SCN5A, HCN4, KCNH2
Specificity
30 %
Genes
19 %
Phosphorus Arrhythmogenic Cardiomyopathy Panel.

By Phosphorus Diagnostics LLC in United States.

DSC2, ACTN2, RBM20, TNNT2, JUP, DSG2, PLN, PRKAG2, TNNI3, TGFB3, RYR2, PKP2, SCN5A, EMD, TMEM43, LDB3, DES, TTN, LMNA, DSP
Specificity
5 %
Genes
7 %
Phosphorus Dilated Cardiomyopathy Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, JUP, DSG2, PLN, TNNI3, TNNC1, ACTC1, RYR2, PKP2, ABCC9, LAMP2, SCN5A, SGCD, TCAP , (...)

View the complete list with 22 more genes
Specificity
5 %
Genes
13 %
Phosphorus Left Ventricular Noncompaction Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, ACTN2, TNNT2, TPM1, PLN, TNNI3, ACTC1, RYR2, LAMP2, SCN5A, HCN4, MYBPC3, LDB3, MYH7, LMNA, TAZ, DSP
Specificity
6 %
Genes
7 %
KCNE2.

By Institute for Human Genetics University Clinic Freiburg in Germany.

KCNE2
Specificity
100 %
Genes
7 %
KCNE2 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

KCNE2
Specificity
100 %
Genes
7 %
Long QT Syndrome via the KCNE2 Gene.

By PreventionGenetics PreventionGenetics in United States.

KCNE2
Specificity
100 %
Genes
7 %
Long QT syndrome type 6.

By Centogene AG - the Rare Disease Company in Germany.

KCNE2
Specificity
100 %
Genes
7 %
KCNE2 gene sequencing.

By Health in Code in Spain.

KCNE2
Specificity
100 %
Genes
7 %
Long QT Syndrome 6.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

KCNE2
Specificity
100 %
Genes
7 %
Atrial fibrillation, familial, 4.

By Praxis fuer Humangenetik Wien in Austria.

KCNE2
Specificity
100 %
Genes
7 %
KCNE2.

By Fulgent Genetics Fulgent Genetics in United States.

KCNE2
Specificity
100 %
Genes
7 %
Long QT syndrome type VI.

By Bioarray in Spain.

KCNE2
Specificity
100 %
Genes
7 %
Long QT syndrome type VI.

By Bioarray in Spain.

KCNE2
Specificity
100 %
Genes
7 %
KCNE2 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

KCNE2
Specificity
100 %
Genes
7 %
KCNE2.

By Institute for Human Genetics University Clinic Freiburg in Germany.

KCNE2
Specificity
100 %
Genes
7 %
KCNE2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

KCNE2
Specificity
100 %
Genes
7 %
Long QT syndrome type 6 (LQT6, sequence analysis of KCNE2 gene).

By CGC Genetics in Portugal.

KCNE2
Specificity
100 %
Genes
7 %
Atrial fibrillation type 4.

By Centogene AG - the Rare Disease Company in Germany.

KCNE2
Specificity
100 %
Genes
7 %
Long QT syndrome 6.

By Praxis fuer Humangenetik Wien in Austria.

KCNE2
Specificity
100 %
Genes
7 %
Atrial fibrillation, familial, 4.

By MedGene in Slovakia.

KCNE2
Specificity
100 %
Genes
7 %
Long QT syndrome 6.

By MedGene in Slovakia.

KCNE2
Specificity
100 %
Genes
7 %
Long QT syndrome type 6: KCNE2 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KCNE2
Specificity
100 %
Genes
7 %
KCNE2 Gene Sequencing and Deletion/Duplication analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

KCNE2
Specificity
100 %
Genes
7 %
Long QT Syndrome Type 6 , Sequencing KCNE2 Gene.

By Reference Laboratory Genetics in Spain.

KCNE2
Specificity
100 %
Genes
7 %
SCN10A.

By Institute for Human Genetics University Clinic Freiburg in Germany.

SCN10A
Specificity
100 %
Genes
7 %
SCN10A. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

SCN10A
Specificity
100 %
Genes
7 %
Familial episodic pain syndrome, 2 (sequencing analysis of SCN10A gene).

By CGC Genetics in Portugal.

SCN10A
Specificity
100 %
Genes
7 %
Comprehensive Epilepsy and Seizure Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

CARS2, KCNH1, SLC1A2, PLPBP, SON, RORB, HCN2, GRIN2D, FRRS1L, CAD, NACC1, TNK2, NPRL2, NPRL3, SCN10A, PIGG, ACY1, GNB1, TUBG1, IER3IP1 , (...)

View the complete list with 133 more genes
Specificity
1 %
Genes
7 %
Familial Episodic Pain Type 2 Syndrome via the SCN10A Gene.

By PreventionGenetics PreventionGenetics in United States.

SCN10A
Specificity
100 %
Genes
7 %
Neuropathy.

By MGZ Medical Genetics Center in Germany.

KLHL13, MICAL1, SH3BP4, LARS, CLP1, DCAF8, ATL3, SCN11A, IFRD1, FAM126A, ARHGEF10, NGF, RETREG1, SCN10A, CHCHD10, SLC52A3, SLC52A2, AAAS, ABCA1, COX10 , (...)

View the complete list with 102 more genes
Specificity
1 %
Genes
7 %
Neuropathic Pain Syndromes Panel.

By CeGaT GmbH in Germany.

TRPA1, SCN11A, SCN10A, SCN9A, NTRK1
Specificity
20 %
Genes
7 %
SCN10A.

By Fulgent Genetics Fulgent Genetics in United States.

SCN10A
Specificity
100 %
Genes
7 %
PAROXYSMAL EXTREME PAIN DISORDER.

By Laboratorio de Genetica Clinica SL in Spain.

SCN11A, SCN10A, SCN9A
Specificity
34 %
Genes
7 %
Paroxysmal Extreme Pain Disorder & Familial Episodic Pain Syndrome , Panel Massive Sequencing (NGS) TRPA1, SCN9A, SCN10A.

By Reference Laboratory Genetics in Spain.

TRPA1, SCN10A, SCN9A
Specificity
34 %
Genes
7 %
Episodic pain syndrome, familial.

By Labor Dr. Wisplinghoff in Germany.

SCN11A, SCN10A
Specificity
50 %
Genes
7 %
Familial episodic pain syndrome, 2 (sequencing analysis of SCN10A gene).

By CGC Genetics in Portugal.

SCN10A
Specificity
100 %
Genes
7 %
Episodic Pain Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

SCN11A, SCN10A, SCN9A
Specificity
34 %
Genes
7 %
SCN10A.

By MGZ Medical Genetics Center in Germany.

SCN10A
Specificity
100 %
Genes
7 %
Episodic pain syndrome type 2, familial.

By Centogene AG - the Rare Disease Company in Germany.

SCN10A
Specificity
100 %
Genes
7 %
Charcot-Marie-Tooth and Sensory Neuropathies Panel.

By CeGaT GmbH in Germany.

DCAF8, ATL3, SCN11A, HOXD10, ARHGEF10, NGF, RETREG1, SCN10A, DST, CCT5, CTDP1, GAN, MED25, AARS, LRSAM1, TFG, HINT1, DHTKD1, GNB4, SBF1 , (...)

View the complete list with 64 more genes
Specificity
2 %
Genes
7 %
CALM2.

By Institute for Human Genetics University Clinic Freiburg in Germany.

CALM2
Specificity
100 %
Genes
7 %
Catecholaminergic polymorphic ventricular tachycardia NGS panel.

By Connective Tissue Gene Tests in United States.

TECRL, CALM3, CASQ2, TRDN, CALM2, CALM1, RYR2, ANK2, KCNJ2
Specificity
45 %
Genes
25 %
Catecholaminergic polymorphic ventricular tachycardia Comprehensive panel.

By Connective Tissue Gene Tests in United States.

TECRL, CALM3, CASQ2, TRDN, CALM2, CALM1, RYR2, ANK2, KCNJ2
Specificity
45 %
Genes
25 %
Ventricular tachycardia, catecholaminergic polymorphic type 3.

By Centogene AG - the Rare Disease Company in Germany.

CALM2
Specificity
100 %
Genes
7 %
Invitae Catecholaminergic Polymorphic Ventricular Tachycardia Panel.

By Invitae in United States.

CALM3, CASQ2, TRDN, CALM2, CALM1, RYR2, ANK2, KCNJ2
Specificity
50 %
Genes
25 %
CALM2.

By Fulgent Genetics Fulgent Genetics in United States.

CALM2
Specificity
100 %
Genes
7 %
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Panel.

By Blueprint Genetics in Finland.

TECRL, CALM3, CASQ2, TRDN, CALM2, CALM1, RYR2, ANK2, KCNJ2
Specificity
45 %
Genes
25 %
Ventricular Tachycardia, Catecholaminergic Polymorphic Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

CASQ2, TRDN, CALM2, CALM1, RYR2, ANK2, KCNJ2
Specificity
58 %
Genes
25 %
CALM2 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

CALM2
Specificity
100 %
Genes
7 %
Phosphorus Catecholaminergic Polymorphic Ventricular Tachycardia Panel.

By Phosphorus Diagnostics LLC in United States.

CALM3, CASQ2, TRDN, CALM2, CALM1, RYR2, ANK2, KCNJ2
Specificity
50 %
Genes
25 %
Long QT Syndrome via the CALM2 Gene.

By PreventionGenetics PreventionGenetics in United States.

CALM2
Specificity
100 %
Genes
7 %
Catecholaminergic polymorphic ventricular tachycardia Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

TECRL, CALM3, CASQ2, TRDN, CALM2, CALM1, RYR2, ANK2, KCNJ2
Specificity
45 %
Genes
25 %
CALM2.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

CALM2
Specificity
100 %
Genes
7 %
AKAP9.

By Institute for Human Genetics University Clinic Freiburg in Germany.

AKAP9
Specificity
100 %
Genes
7 %
Long QT syndrome 11 (sequence analysis of AKAP9 gene).

By CGC Genetics in Portugal.

AKAP9
Specificity
100 %
Genes
7 %
Long QT Syndrome via the AKAP9 Gene.

By PreventionGenetics PreventionGenetics in United States.

AKAP9
Specificity
100 %
Genes
7 %
Long QT Syndrome 11.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

AKAP9
Specificity
100 %
Genes
7 %
AKAP9.

By Fulgent Genetics Fulgent Genetics in United States.

AKAP9
Specificity
100 %
Genes
7 %
AKAP9 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

AKAP9
Specificity
100 %
Genes
7 %
Caris MI TumorSeek 592-Gene NGS Panel.

By Caris Life Sciences in United States.

ETV1, BCL3, SET, ELL, BTG1, ADGRA2, ACSL3, AFF1, ACSL6, ACKR3, RABEP1, PSIP1, RANBP17, RAD51B, RPL22, SDC4, SH3GL1, REL, SLC45A3, SYK , (...)

View the complete list with 571 more genes
Specificity
1 %
Genes
13 %
CEN4GEN Prostate cancer: Extended gene sequencing Panel.

By CEN4GEN Institute for Genomics and Molecular Diagnostics in Canada.

SPOP, ZNF473, THSD7B, ZNF595, KDM4B, NRCAM, OR5L1, PDZRN3, NKX3-1, NIPA2, KLF6, GLI1, MYC, CDK12, SCN11A, TBX20, PIK3CA, CDKN1B, AKAP9, MED12 , (...)

View the complete list with 8 more genes
Specificity
4 %
Genes
7 %
Long QT syndrome type 11.

By Centogene AG - the Rare Disease Company in Germany.

AKAP9
Specificity
100 %
Genes
7 %
Long QT syndrome type XI.

By Bioarray in Spain.

AKAP9
Specificity
100 %
Genes
7 %
AKAP9 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

AKAP9
Specificity
100 %
Genes
7 %
Familial hyperaldosteronism type III (sequence analysis of KCNJ5 gene).

By CGC Genetics in Portugal.

KCNJ5
Specificity
100 %
Genes
7 %
Hyperaldosteronism, familial, type III.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

KCNJ5
Specificity
100 %
Genes
7 %
Hereditary kidney disorders - different panels.

By Institute of Human Genetics Cologne University in Germany.

CLDN10, TMEM260, KANK3, SLC6A20, MAGEC1, TBC1D1, SLC41A1, SLC36A2, SLC22A10, KCNMB1, NRIP1, MAGED2, DYNC2LI1, IFT52, RMND1, MAPKBP1, MOCOS, SLC26A1, PDE3A, FN1 , (...)

View the complete list with 391 more genes
Specificity
1 %
Genes
7 %
Long QT syndrome type 13.

By Centogene AG - the Rare Disease Company in Germany.

KCNJ5
Specificity
100 %
Genes
7 %
Hyperaldosteronism, familial, type III.

By Centogene AG - the Rare Disease Company in Germany.

KCNJ5
Specificity
100 %
Genes
7 %
Bartter Syndrome incl. differential diagnosis Panel.

By CeGaT GmbH in Germany.

KCNJ18, KCNJ5, KCNE3, KCNJ2, CACNA1S, SCN4A
Specificity
17 %
Genes
7 %
Single gene testing KCNJ5.

By CeGaT GmbH in Germany.

KCNJ5
Specificity
100 %
Genes
7 %
Periodic paralysis Panel.

By CeGaT GmbH in Germany.

KCNJ5, KCNE3, KCNJ2, CACNA1S, SCN4A
Specificity
20 %
Genes
7 %
Long QT Syndrome 13.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

KCNJ5
Specificity
100 %
Genes
7 %
KidneySeq - 264 Genes.

By Iowa Institute of Human Genetics University of Iowa in United States.

FN1, FAN1, DSTYK, CHD1L, SIX2, ARHGAP24, NUP107, NUP93, NUP205, FAT1, XPO5, SGPL1, TRAP1, UPK3A, AGTR1, TBX18, EHHADH, ANLN, FGF20, KCTD1 , (...)

View the complete list with 232 more genes
Specificity
1 %
Genes
7 %
Pseudohypoaldosteronism Panel.

By Blueprint Genetics in Finland.

WNK4, CUL3, KLHL3, NR3C2, KCNJ5, SCNN1B, SCNN1G, SCNN1A, HSD11B2, WNK1
Specificity
10 %
Genes
7 %
Hyperaldosteronism, familial, type III.

By Bioarray in Spain.

KCNJ5
Specificity
100 %
Genes
7 %
KCNJ5 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

KCNJ5
Specificity
100 %
Genes
7 %
KCNJ5.

By Institute for Human Genetics University Clinic Freiburg in Germany.

KCNJ5
Specificity
100 %
Genes
7 %
KCNJ5.

By Institute for Human Genetics University Clinic Freiburg in Germany.

KCNJ5
Specificity
100 %
Genes
7 %
KCNJ5 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

KCNJ5
Specificity
100 %
Genes
7 %
KCNJ5. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

KCNJ5
Specificity
100 %
Genes
7 %
Long QT syndrome 13 (sequence analysis of KCNJ5 gene).

By CGC Genetics in Portugal.

KCNJ5
Specificity
100 %
Genes
7 %
Familial hyperaldosteronism type III (sequence analysis of KCNJ5 gene).

By CGC Genetics in Portugal.

KCNJ5
Specificity
100 %
Genes
7 %
Hyperaldosteronism, familial, type III.

By Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders in Germany.

KCNJ5
Specificity
100 %
Genes
7 %
Long QT Syndrome via KCNJ5 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

KCNJ5
Specificity
100 %
Genes
7 %
Primary Aldosteronism Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

KCNJ5, CACNA1D, CACNA1H
Specificity
34 %
Genes
7 %
Hyperaldosteronism.

By Institute of Human Genetics Cologne University in Germany.

RMND1, KCNJ5
Specificity
50 %
Genes
7 %
Hypertension.

By Institute of Human Genetics Cologne University in Germany.

PDE3A, WNK4, CUL3, KLHL3, NR3C2, KCNJ5, SCNN1G, SCNN1A, HSD11B2, WNK1, SDHD, SDHA, CYP17A1, SDHB, SDHC, SDHAF2
Specificity
7 %
Genes
7 %
Hyperaldosteronism, familial, type III: KCNJ5 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KCNJ5
Specificity
100 %
Genes
7 %
KCNJ5.

By Fulgent Genetics Fulgent Genetics in United States.

KCNJ5
Specificity
100 %
Genes
7 %
Long QT syndrome type XIII.

By Bioarray in Spain.

KCNJ5
Specificity
100 %
Genes
7 %
KCNJ5 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

KCNJ5
Specificity
100 %
Genes
7 %
Familial Hyperaldosteronism Type III , Sequencing KCNJ5 Gene.

By Reference Laboratory Genetics in Spain.

KCNJ5
Specificity
100 %
Genes
7 %
Caveolin 3 (CAV3) DNA Sequencing Test.

By Athena Diagnostics Inc in United States.

CAV3
Specificity
100 %
Genes
7 %
Distal Myopathy Advanced Sequencing Evaluation.

By Athena Diagnostics Inc in United States.

MATR3, LDB3, TIA1, MYOT, ANO5, FLNC, MYH7, DES, KLHL9, TTN, DYSF, CAV3, DNM2, NEB, VCP, CRYAB, GNE
Specificity
6 %
Genes
7 %
Limb Girdle Muscular Dystrophy Advanced Evaluation.

By Athena Diagnostics Inc in United States.

SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, MYOT, ANO5, DES, TTN, DYSF, CAV3, FKRP, LMNA, CAPN3, SGCG, POMGNT1, SGCB , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
7 %
Neuromuscular Disorders Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

GMPPB, LMOD3, SPEG, STAC3, POMK, TOR1AIP1, SLC5A7, HNRNPDL, MTMR14, TNNI2, TNPO3, MYF6, LIMS2, KLHL41, GLE1, COL12A1, AMPD1, FBXL4, GAN, HINT1 , (...)

View the complete list with 124 more genes
Specificity
1 %
Genes
7 %
NGS Rhabdomyolysis and Metabolic Myopathies Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

PGK1, CTDP1, MT-CYB, CASQ1, FDX2, AMPD1, TSEN54, SIL1, RYR1, ATP2A1, ANO5, SCN4A, DYSF, CAV3, FKRP, FKTN, DMD, SLC25A20, ETFDH, ETFA , (...)

View the complete list with 27 more genes
Specificity
3 %
Genes
7 %
Hypertrophic cardiomyopathy - full panel.

By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario in Canada.

MYL3, MYL2, CSRP3, ACTN2, MYOZ2, TNNT2, TPM1, NEXN, PLN, PRKAG2, TNNI3, TNNC1, ACTC1, LAMP2, MYBPC3, MYH7, CAV3, GLA, TTR
Specificity
6 %
Genes
7 %
Hypertrophic cardiomyopathy - familial variant analysis.

By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario in Canada.

MYL3, MYL2, CSRP3, ACTN2, MYOZ2, TNNT2, TPM1, NEXN, PLN, PRKAG2, TNNI3, TNNC1, ACTC1, LAMP2, MYBPC3, MYH7, CAV3, GLA, TTR
Specificity
6 %
Genes
7 %
Comprehensive Neuromuscular Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

MTMR14, TNNI2, GLE1, AMPD1, PLEKHG5, RYR2, CHRNG, ITGA7, COL6A1, LARGE1, COL6A3, COL6A2, LAMA2, SIL1, CHRNB1, CHRND, CHRNA1, MUSK, COLQ, ISPD , (...)

View the complete list with 59 more genes
Specificity
2 %
Genes
7 %
Limb-Girdle Muscular Dystrophy.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

COL6A1, COL6A3, COL6A2, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, EMD, SYNE2, SYNE1, FHL1, MYOT, ANO5, FLNC, DES, TTN, DYSF , (...)

View the complete list with 14 more genes
Specificity
3 %
Genes
7 %
Hypertrophic Cardiomyopathy Panel (23 genes).

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

VCL, MYL3, MYL2, CSRP3, ACTN2, TNNT2, TPM1, NEXN, PLN, PRKAG2, TNNI3, TNNC1, ANKRD1, ACTC1, LAMP2, MYBPC3, LDB3, CAV3, SURF1, SCO2 , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
7 %
CAV3 Sequencing.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

CAV3
Specificity
100 %
Genes
7 %
Limb-Girdle Muscular Dystrophy Deletion/Duplication Panel.

By Genetic Services Laboratory University of Chicago in United States.

GMPPB, POMK, HNRNPDL, TNPO3, LIMS2, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, MYOT, ANO5, FLNC, DES, TTN, DYSF , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
7 %
CAV3.

By Institute for Human Genetics University Clinic Freiburg in Germany.

CAV3
Specificity
100 %
Genes
7 %
Caveolinopathies (sequence analysis of CAV3).

By CGC Genetics in Portugal.

CAV3
Specificity
100 %
Genes
7 %
Hypertrophic cardiomyopathy (HCM, NGS panel for 22 genes).

By CGC Genetics in Portugal.

VCL, MYL3, MYL2, CSRP3, MYOZ2, TNNT2, TPM1, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, MYLK2, ACTC1, LAMP2, TCAP, MYBPC3, MYH7, TTN , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
7 %
Non-dystrophic myotonias (NGS panel for 11 genes).

By CGC Genetics in Portugal.

KCNJ18, HINT1, KCNE3, KCNA1, CACNA1S, HSPG2, ATP2A1, CACNA1A, SCN4A, CAV3, CLCN1
Specificity
10 %
Genes
7 %
Cardiomyopathy (hypertrophic, dilated and arrhythmogenic right ventricular dysplasia, NGS panel for 36 genes).

By CGC Genetics in Portugal.

VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, TNNT2, TPM1, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, MYLK2, ACTC1 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
7 %
Caveolinopathies.

By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine in United States.

CAV3
Specificity
100 %
Genes
7 %
CAV3-Related Sudden Infant Death Syndrome.

By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine in United States.

CAV3
Specificity
100 %
Genes
7 %
Long QT Syndrome 9.

By John Welsh Cardiovascular Diagnostic Laboratory Baylor College of Medicine in United States.

CAV3
Specificity
100 %
Genes
7 %
Limb-Girdle Muscular Dystrophy (LGMD) Sequencing Panel.

By PreventionGenetics PreventionGenetics in United States.

GMPPB, POMK, TOR1AIP1, HNRNPDL, TNPO3, LIMS2, SMCHD1, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DNAJB6, TRAPPC11, MYOT, ANO5, DES, TTN, DYSF , (...)

View the complete list with 13 more genes
Specificity
4 %
Genes
7 %
Caveolinopathy via the CAV3 Gene.

By PreventionGenetics PreventionGenetics in United States.

CAV3
Specificity
100 %
Genes
7 %
Comprehensive Neuromuscular Sequencing Panel.

By PreventionGenetics PreventionGenetics in United States.

MYO18B, HNRNPA1, HNRNPA2B1, ALG14, PREPL, SYT2, COL13A1, MICU1, STIM1, ECEL1, MYH3, TNNT3, GMPPB, LMOD3, STAC3, POMK, TOR1AIP1, HNRNPDL, TNNI2, TNPO3 , (...)

View the complete list with 104 more genes
Specificity
1 %
Genes
7 %
Distal Myopathy NGS panel.

By Connective Tissue Gene Tests in United States.

TCAP, DNAJB6, FHL1, BAG3, MATR3, LDB3, TIA1, MYOT, ANO5, FLNC, MYH7, DES, TTN, DYSF, CAV3, DNM2, SQSTM1, VCP, CRYAB, GNE
Specificity
5 %
Genes
7 %
Distal Myopathy Comprehensive panel.

By Connective Tissue Gene Tests in United States.

TCAP, DNAJB6, FHL1, BAG3, MATR3, LDB3, TIA1, MYOT, ANO5, FLNC, MYH7, DES, TTN, DYSF, CAV3, DNM2, SQSTM1, VCP, CRYAB, GNE
Specificity
5 %
Genes
7 %
Distal Myopathy Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

TCAP, DNAJB6, FHL1, BAG3, MATR3, LDB3, TIA1, MYOT, ANO5, FLNC, MYH7, DES, TTN, DYSF, CAV3, DNM2, SQSTM1, VCP, CRYAB, GNE
Specificity
5 %
Genes
7 %
Limb girdle muscular dystrophy Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

GMPPB, POMK, TOR1AIP1, HNRNPDL, TNPO3, LIMS2, LARGE1, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, EMD, FHL1, MYOT, ANO5 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
7 %
Myotonia.

By MGZ Medical Genetics Center in Germany.

HINT1, ACTA1, HSPG2, SCN4A, CAV3, CLCN1, CAVIN1, GAA
Specificity
13 %
Genes
7 %
Muscle Disease with Distal Myopathy.

By MGZ Medical Genetics Center in Germany.

MYH14, CHRNB1, CHRND, CHRNA1, AGRN, TCAP, BICD2, CCDC78, FHL1, BAG3, MATR3, LDB3, TIA1, MYOT, ANO5, FLNC, MYH7, DES, TTN, DYSF , (...)

View the complete list with 8 more genes
Specificity
4 %
Genes
7 %
Muscle Weakness (Myopathy, Muscular Dystrophy).

By MGZ Medical Genetics Center in Germany.

SLC6A5, GLRA1, GLRB, SLC52A3, ALG14, LRP4, PREPL, MICU1, ORAI1, STIM1, HADH, PGK1, FDX2, MYBPC1, PIEZO2, GMPPB, STAC3, POMK, TOR1AIP1, MTMR14 , (...)

View the complete list with 159 more genes
Specificity
1 %
Genes
7 %
Caveolinopathy Testing.

By FirmaLab in United States.

CAV3
Specificity
100 %
Genes
7 %
Distal Myopathy Panel.

By FirmaLab in United States.

MATR3, LDB3, MYOT, ANO5, MYH7, TTN, DYSF, CAV3, DNM2, NEB, GNE
Specificity
10 %
Genes
7 %
Myotonia Panel.

By CeGaT GmbH in Germany.

HINT1, ATP2A1, SCN4A, CAV3, CLCN1
Specificity
20 %
Genes
7 %
Caveolinopathies.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

CAV3
Specificity
100 %
Genes
7 %
Rippling muscle disease.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

CAV3
Specificity
100 %
Genes
7 %
Limb girdle muscular dystrophy-Panel.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SGCD, TCAP, POMT1, POMT2, DNAJB6, MYOT, ANO5, DES, DYSF, CAV3, LMNA, CAPN3, SGCG, SGCB, SGCA, FKTN, DMD, TRIM32
Specificity
6 %
Genes
7 %
Hypertrophic Cardiomyopathy.

By Asper Biogene Asper Biogene LLC in Estonia.

CALR3, VCL, MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, MYPN, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, MYLK2, ACTC1, LAMP2 , (...)

View the complete list with 8 more genes
Specificity
4 %
Genes
7 %
Limb-Girdle Muscular Dystrophy.

By Asper Biogene Asper Biogene LLC in Estonia.

GMPPB, POMK, HNRNPDL, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, MYOT, ANO5, DES, TTN, DYSF, CAV3, LMNA, CAPN3 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
7 %
Skeletal Myopathy Panel.

By Health in Code in Spain.

CAVIN4, MYL3, MYL2, PRKAG2, TNNI3, KCNE3, LAMP2, CACNA1C, LAMA2, KCNJ2, SGCD, TCAP, EMD, TMEM43, ACTA1, FHL1, BAG3, BSCL2, LDB3, MYOT , (...)

View the complete list with 26 more genes
Specificity
3 %
Genes
7 %
Hypertrophic Cardiomyopathy Extended Panel.

By Health in Code in Spain.

FHOD3, TRIM63, KLF10, CALR3, CAVIN4, OBSL1, AGPAT2, FHL2, CTF1, VCL, MYL3, MYL2, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, MYPN, NEXN, PLN , (...)

View the complete list with 70 more genes
Specificity
3 %
Genes
13 %
Long QT Syndrome 9.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

CAV3
Specificity
100 %
Genes
7 %
Cardiomyopathy, familial hypertrophic.

By Praxis fuer Humangenetik Wien in Austria.

CAV3
Specificity
100 %
Genes
7 %
Muscular dystrophy, limb-girdle 1C.

By Praxis fuer Humangenetik Wien in Austria.

CAV3
Specificity
100 %
Genes
7 %
Myopathy, distal, Tateyama type.

By Praxis fuer Humangenetik Wien in Austria.

CAV3
Specificity
100 %
Genes
7 %
Rippling muscle disease.

By Praxis fuer Humangenetik Wien in Austria.

CAV3
Specificity
100 %
Genes
7 %
Cardiomyopathy, familial hypertrophic.

By MedGene in Slovakia.

CAV3
Specificity
100 %
Genes
7 %
Long QT syndrome 9.

By MedGene in Slovakia.

CAV3
Specificity
100 %
Genes
7 %
Myopathy, distal, Tateyama type.

By MedGene in Slovakia.

CAV3
Specificity
100 %
Genes
7 %
Invitae Comprehensive Myopathy Panel.

By Invitae in United States.

STIM1, LMOD3, STAC3, KLHL41, MYL2, MYPN, FKBP14, COL6A1, COL6A3, COL6A2, KCNJ2, DNAJB6, BIN1, MTM1, TNNT1, TPM2, CFL2, CNTN1, KBTBD13, MEGF10 , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
7 %
Invitae Limb-Girdle Muscular Dystrophy Panel.

By Invitae in United States.

GMPPB, POMK, TNPO3, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, MYOT, ANO5, DES, TTN, DYSF, CAV3, FKRP, LMNA , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
7 %
LIMB-GIRDLE MUSCULAR DYSTROPHY, A.D..

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

DNAJB6, MYOT, DES, CAV3, LMNA
Specificity
20 %
Genes
7 %
Non-dystrophic myotonias.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KCNJ18, HINT1, KCNE3, KCNA1, CACNA1S, HSPG2, ATP2A1, CACNA1A, SCN4A, CAV3, CLCN1
Specificity
10 %
Genes
7 %
Limb-Girdle Muscular Dystrophy Type 1C: CAV3 Full Gene Sequencing.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

CAV3
Specificity
100 %
Genes
7 %
Hypertrophic Cardiomyopathy: Sequencing and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MYL3, MYL2, MYOZ2, JPH2, TNNT2, TPM1, MYPN, PRKAG2, MYH6, TNNI3, TNNC1, ACTC1, LAMP2, MYBPC3, MYH7, TTN, CAV3, GLA, TTR
Specificity
6 %
Genes
7 %
Neuromuscular Disorders: Gene Sequencing and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

AMPD3, TNNI2, AMPD1, RYR2, ITGA7, COL6A1, LARGE1, COL6A3, COL6A2, LAMA2, SIL1, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, EMD, TNNT1, TPM2 , (...)

View the complete list with 26 more genes
Specificity
3 %
Genes
7 %
Limb-Girdle Muscular Dystrophy: Sequencing and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

COL6A1, COL6A3, COL6A2, SMCHD1, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, SYNE2, SYNE1, FHL1, MYOT, ANO5, FLNC, DES, TTN, DYSF , (...)

View the complete list with 14 more genes
Specificity
3 %
Genes
7 %
Muscular Dystrophies NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MMEL1, SGCD, TCAP, POMT1, POMT2, DAG1, DNAJB6, EMD, SYNE2, TMEM43, SYNE1, FHL1, MYOT, ANO5, DES, TTN, DYSF, CAV3, FKRP, LMNA , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
7 %
CAV3.

By Fulgent Genetics Fulgent Genetics in United States.

CAV3
Specificity
100 %
Genes
7 %
Comprehensive Metabolism Panel.

By Blueprint Genetics in Finland.

PRKAG3, NIPA2, GLUL, SLC6A9, SLC25A26, ADK, GMPPA, TANGO2, COQ5, COQ7, MOCOS, FLAD1, CTH, DPYS, UPB1, ALAD, ABCD3, STT3A, STT3B, NGLY1 , (...)

View the complete list with 414 more genes
Specificity
1 %
Genes
7 %
Metabolic Myopathy and Rhabdomyolysis Panel.

By Blueprint Genetics in Finland.

TANGO2, FLAD1, GYG1, RBCK1, PGK1, MYH3, AMPD1, RYR1, ANO5, SCN4A, DYSF, CAV3, FKRP, FKTN, AHCY, SLC25A20, SLC22A5, ETFDH, ETFA, ETFB , (...)

View the complete list with 32 more genes
Specificity
2 %
Genes
7 %
Long QT syndrome type IX.

By Bioarray in Spain.

CAV3
Specificity
100 %
Genes
7 %
Autosomal dominant limb-girdle muscular dystrophy type 1C.

By Bioarray in Spain.

CAV3
Specificity
100 %
Genes
7 %
Wolff-Parkinson White Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, ANKRD1, ACTC1, LAMP2, TCAP, MYBPC3, MYH7 , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
7 %
Cardiomyopathy, familial hypertrophic Panel by NGS.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, ANKRD1, ACTC1, LAMP2, TCAP, MYBPC3, MYH7 , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
7 %
FAMILIAL HYPERTROPHIC CARDIOMYOPATHY.

By Laboratorio de Genetica Clinica SL in Spain.

VCL, MYL3, MYL2, CSRP3, ACTN2, TNNT2, TPM1, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, MYLK2, ACTC1, TCAP, MYBPC3, MYH7, TTN, CAV3
Specificity
5 %
Genes
7 %
MUSCULAR DYSTROPHY, LIMB-GIRDLE:NGS NGS PANEL.

By Laboratorio de Genetica Clinica SL in Spain.

GMPPB, HNRNPDL, TNPO3, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, MYOT, ANO5, DES, TTN, DYSF, CAV3, FKRP, LMNA, CAPN3 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
7 %
Limb-girdle muscular dystrophy panel.

By LifeLabs Genetics in Canada.

SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, MYOT, ANO5, DES, TTN, DYSF, CAV3, FKRP, LMNA, CAPN3, SGCG, POMGNT1, SGCB, SGCA , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
7 %
Familial Hypertrophic Cardiomyopathy, Panel Massive Sequencing (NGS) 37 Genes.

By Reference Laboratory Genetics in Spain.

CALR3, VCL, MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, MYPN, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, MYLK2, ACTC1, RYR2 , (...)

View the complete list with 17 more genes
Specificity
6 %
Genes
13 %
Limb-Girdle Muscular Distrophy , Panel Massive Sequencing (NGS) 22 Genes.

By Reference Laboratory Genetics in Spain.

SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, MYOT, ANO5, DES, TTN, DYSF, CAV3, FKRP, LMNA, CAPN3, SGCG, POMGNT1, SGCB, SGCA , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
7 %
Non-Dystrophic Myotonias , Panel Massive Sequencing (NGS) 9 Genes.

By Reference Laboratory Genetics in Spain.

KCNE3, KCNA1, CACNA1S, HSPG2, ATP2A1, CACNA1A, SCN4A, CAV3, CLCN1
Specificity
12 %
Genes
7 %
Muscle Polyneuropathies , Panel Massive Sequencing (NGS) 111 Genes.

By Reference Laboratory Genetics in Spain.

AMPD3, PEX11B, TNNT3, MTMR14, TNNI2, GLE1, AMPD1, PLEKHG5, RYR2, LAMP2, CHRNG, PEX5, PEX12, PEX10, PEX26, PEX3, PEX14, CACNA1C, PEX6, ITGA7 , (...)

View the complete list with 91 more genes
Specificity
1 %
Genes
7 %
Phosphorus Hypertrophic Cardiomyopathy Including Rasopathies Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, MYL3, MYL2, CSRP3, ACTN2, TNNT2, TPM1, PLN, PRKAG2, TNNI3, TNNC1, ACTC1, A2ML1, RRAS, SPRED1, LAMP2, RASA1, CACNA1C, TCAP, MYBPC3 , (...)

View the complete list with 25 more genes
Specificity
3 %
Genes
7 %
Phosphorus Hypertrophic Cardiomyopathy Including Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, MYL3, MYL2, CSRP3, ACTN2, TNNT2, TPM1, PLN, PRKAG2, TNNI3, TNNC1, ACTC1, LAMP2, CACNA1C, TCAP, MYBPC3, FHL1, BAG3, LDB3, FLNC , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
7 %
Myotonic Syndrome Advanced Evaluation.

By Athena Diagnostics Inc in United States.

HSPG2, ATP2A1, SCN4A, CNBP, CAV3, CLCN1, DMPK
Specificity
15 %
Genes
7 %
Muscular Dystrophy Advanced Evaluation.

By Athena Diagnostics Inc in United States.

SMCHD1, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, EMD, SYNE2, TMEM43, SYNE1, CCDC78, FHL1, MYOT, ANO5, DES, TTN , (...)

View the complete list with 13 more genes
Specificity
4 %
Genes
7 %
NGS Rhabdomyolysis and Metabolic Myopathies Panel.

By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.

PGK1, CTDP1, MT-CYB, CASQ1, FDX2, AMPD1, TSEN54, SIL1, RYR1, ATP2A1, ANO5, SCN4A, DYSF, CAV3, FKRP, FKTN, DMD, SLC25A20, ETFDH, ETFA , (...)

View the complete list with 27 more genes
Specificity
3 %
Genes
7 %
Pan-cardiomyopathy panel.

By CHEO Genetics Diagnostic Laboratory Children's Hospital of Eastern Ontario in Canada.

FHL2, CTF1, VCL, MYL3, MYL2, DSC2, CSRP3, ACTN2, RBM20, MYOZ2, TNNT2, TPM1, JUP, DSG2, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1 , (...)

View the complete list with 25 more genes
Specificity
3 %
Genes
7 %
Hypertrophic Cardiomyopathy Panel.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

OBSCN, VCL, MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, MYPN, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, ANKRD1, MYLK2, ACTC1 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
7 %
Neuromuscular Disorders Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

ALG14, LRP4, PREPL, SYT2, HACD1, COL13A1, ORAI1, STIM1, GMPPB, LMOD3, SPEG, STAC3, POMK, HNRNPDL, TNPO3, MYF6, LIMS2, KLHL41, COL12A1, MYL2 , (...)

View the complete list with 91 more genes
Specificity
1 %
Genes
7 %
Limb-Girdle Muscular Dystrophy Sequencing Panel.

By Genetic Services Laboratory University of Chicago in United States.

GMPPB, POMK, HNRNPDL, TNPO3, LIMS2, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, MYOT, ANO5, FLNC, DES, TTN, DYSF , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
7 %
Muscular dystrophy, limb-girdle, type IC.

By Human Genetics Ruhr University in Germany.

CAV3
Specificity
100 %
Genes
7 %
HCM Sequencing Panel.

By GeneDx in United States.

MT-TQ, MT-TI, MT-TG, MYL3, MYL2, TNNT2, TPM1, PRKAG2, TNNI3, TNNC1, ACTC1, LAMP2, MYBPC3, MYH7, CAV3, MT-TK, GLA, TTR
Specificity
6 %
Genes
7 %
Rhabdomyolysis.

By Sheffield Diagnostic Genetics Service Sheffield Children's NHS Foundation Trust in United Kingdom.

GYG1, PHKG1, FBP2, RBCK1, PGK1, RYR1, CAV3, CPT1B, SLC22A5, ETFDH, ETFA, ETFB, GBE1, PYGM, PFKM, ISCU, PGAM2, LPIN1, PHKA1, HADHB , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
7 %
CAV3 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

CAV3
Specificity
100 %
Genes
7 %
CAV3. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

CAV3
Specificity
100 %
Genes
7 %
Limb-girdle muscular dystrophies (NGS panel for 26 genes).

By CGC Genetics in Portugal.

GMPPB, HNRNPDL, TNPO3, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, MYOT, ANO5, DES, TTN, DYSF, CAV3, FKRP, LMNA, CAPN3 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
7 %
CAVEOLINOPATHY.

By Centre de Genetique Humaine Institut de Pathologie et de Genetique in Belgium.

CAV3
Specificity
100 %
Genes
7 %
Distal Hereditary Myopathy Sequencing Panel.

By PreventionGenetics PreventionGenetics in United States.

TCAP, DNAJB6, FHL1, BAG3, MATR3, LDB3, TIA1, MYOT, ANO5, FLNC, MYH7, DES, KLHL9, TTN, DYSF, CAV3, SQSTM1, VCP, CRYAB, GNE
Specificity
5 %
Genes
7 %
Hypertrophic Cardiomyopathy Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

VCL, MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, MYPN, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, ANKRD1, MYLK2, ACTC1, RYR2 , (...)

View the complete list with 18 more genes
Specificity
3 %
Genes
7 %
Limb girdle muscular dystrophy Comprehensive panel.

By Connective Tissue Gene Tests in United States.

GMPPB, POMK, TOR1AIP1, HNRNPDL, TNPO3, LIMS2, LARGE1, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, EMD, FHL1, MYOT, ANO5 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
7 %
Limb girdle muscular dystrophy NGS panel.

By Connective Tissue Gene Tests in United States.

GMPPB, POMK, TOR1AIP1, HNRNPDL, TNPO3, LIMS2, LARGE1, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, EMD, FHL1, MYOT, ANO5 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
7 %
Muscular Dystrophy: Limb Girdle - autosomal dominant.

By MGZ Medical Genetics Center in Germany.

DNAJB6, MYOT, DES, CAV3, LMNA
Specificity
20 %
Genes
7 %
Caveolinopathies CAV3.

By MGZ Medical Genetics Center in Germany.

CAV3
Specificity
100 %
Genes
7 %
Pulmonary diseases - panels.

By MGZ Medical Genetics Center in Germany.

TBX4, DVL1, COL4A2, EIF2AK4, NOTCH2, DNAI1, BMPR2, DNAH5, NME8, DNAH11, DNAI2, DNAAF2, RSPH4A, RSPH9, DNAAF1, DNAAF3, SMAD9, CAV1, KCNK3, DNAAF4 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
7 %
Muscle Weakness Manifesting in Adulthood / Limb-Girdle Muscular Dystrophy (AD and AR).

By MGZ Medical Genetics Center in Germany.

STIM1, HADH, GMPPB, TOR1AIP1, TNPO3, LIMS2, HINT1, LAMP2, HNRNPU, COL6A1, LARGE1, COL6A3, COL6A2, CHKB, CHRNB1, CHRND, CHRNA1, GFPT1, COLQ, SGCD , (...)

View the complete list with 70 more genes
Specificity
2 %
Genes
7 %
Myopathy, distal with decreased Caveolin 3.

By Centogene AG - the Rare Disease Company in Germany.

CAV3
Specificity
100 %
Genes
7 %
Limb-girdle muscular dystrophy, autosomal dominant type 1C.

By Centogene AG - the Rare Disease Company in Germany.

CAV3
Specificity
100 %
Genes
7 %
Long QT syndrome type 9.

By Centogene AG - the Rare Disease Company in Germany.

CAV3
Specificity
100 %
Genes
7 %
Limb-girdle muscular dystrophy panel.

By Centogene AG - the Rare Disease Company in Germany.

SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, MYOT, ANO5, TTN, DYSF, CAV3, FKRP, LMNA, CAPN3, SGCG, POMGNT1, SGCB, SGCA, FKTN , (...)

View the complete list with 1 more genes
Specificity
5 %
Genes
7 %
Cardiomyopathy, familial hypertrophic.

By Centogene AG - the Rare Disease Company in Germany.

CAV3
Specificity
100 %
Genes
7 %
Creatine phosphokinase, elevated serum.

By Centogene AG - the Rare Disease Company in Germany.

CAV3
Specificity
100 %
Genes
7 %
Rippling muscle disease.

By Centogene AG - the Rare Disease Company in Germany.

CAV3
Specificity
100 %
Genes
7 %
Non-dystrophic myotonia congenita panel.

By Centogene AG - the Rare Disease Company in Germany.

HINT1, KCNE3, KCNA1, CACNA1S, HSPG2, ATP2A1, CACNA1A, SCN4A, CAV3, CLCN1
Specificity
10 %
Genes
7 %
Congenital and Distal Myopathies Panel.

By CeGaT GmbH in Germany.

HNRNPA1, HNRNPA2B1, MSTN, VMA21, CHCHD10, HACD1, MICU1, ORAI1, STIM1, CASQ1, LMOD3, SPEG, STAC3, MTMR14, MYF6, KLHL41, COL12A1, DNA2, ACVR1, FKBP14 , (...)

View the complete list with 53 more genes
Specificity
2 %
Genes
7 %
Cardiomyopathy, hypertrophic Panel.

By CeGaT GmbH in Germany.

CALR3, VCL, MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, MYPN, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, ANKRD1, MYLK2, ACTC1 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
7 %
Limb-Girdle Muscular Dystrophies Panel.

By CeGaT GmbH in Germany.

GMPPB, POMK, HNRNPDL, TNPO3, LAMA2, ISPD, SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, TRAPPC11, MYOT, ANO5, FLNC, DES, TTN, DYSF , (...)

View the complete list with 14 more genes
Specificity
3 %
Genes
7 %
Limb-Girdle Muscular Dystrophy type 1.

By Laboratory of Human Genetics GENOMED Health Care Center in Poland.

HNRNPDL, TNPO3, DNAJB6, MYOT, DES, CAV3, LMNA
Specificity
15 %
Genes
7 %
Long QT Syndrome 9.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

CAV3
Specificity
100 %
Genes
7 %
Limb girdle muscular dystrophy 1C.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

CAV3
Specificity
100 %
Genes
7 %
Metabolic Myopathy and Rhabdomyolysis.

By Asper Biogene Asper Biogene LLC in Estonia.

GYG1, PGK1, AMPD1, PRKAG2, RYR1, CAV3, SLC25A20, SLC22A5, ETFDH, ETFA, ETFB, GBE1, PYGM, PFKM, ISCU, PGAM2, LPIN1, ABHD5, PHKA1, TAZ , (...)

View the complete list with 23 more genes
Specificity
3 %
Genes
7 %
Congenital Myopathy and Distal Myopathy NGS panel.

By Asper Biogene Asper Biogene LLC in Estonia.

MICU1, LMOD3, STAC3, MTMR14, MYF6, KLHL41, COL12A1, COL6A1, COL6A3, DNAJB6, MTM1, TNNT1, TPM2, CFL2, CNTN1, MEGF10, CCDC78, ACTA1, TPM3, KLHL40 , (...)

View the complete list with 21 more genes
Specificity
3 %
Genes
7 %
CAV3 gene sequencing.

By Health in Code in Spain.

CAV3
Specificity
100 %
Genes
7 %
Skeletal myopathy Panel.

By Health in Code in Spain.

CAVIN4, XK, SPEG, TOR1AIP1, MYL3, MYL2, PRKAG2, TNNI3, KCNE3, LAMP2, CACNA1C, LAMA2, KCNJ2, SGCD, TCAP, EMD, SYNE2, TMEM43, SYNE1, ACTA1 , (...)

View the complete list with 37 more genes
Specificity
2 %
Genes
7 %
Dilated Cardiomyopathy Panel.

By Health in Code in Spain.

FHOD3, CHRM2, COL7A1, FHL2, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, DSG2, PLN, TNNI3, TNNC1, ANKRD1, ACTC1, PKP2, ABCC9, EMD, ACTA1 , (...)

View the complete list with 19 more genes
Specificity
3 %
Genes
7 %
Hypertrophic cardiomyopathy extended panel.

By Health in Code in Spain.

MYOM1, FHOD3, MRPL44, COA6, TRIM63, KLF10, CALR3, CAVIN4, COA5, OBSL1, AGPAT2, OBSCN, FHL2, VCL, MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2 , (...)

View the complete list with 84 more genes
Specificity
2 %
Genes
13 %
Caveolinopathies.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

CAV3
Specificity
100 %
Genes
7 %
Creatine phosphokinase, elevated serum.

By Praxis fuer Humangenetik Wien in Austria.

CAV3
Specificity
100 %
Genes
7 %
Long QT syndrome 9.

By Praxis fuer Humangenetik Wien in Austria.

CAV3
Specificity
100 %
Genes
7 %
Creatine phosphokinase, elevated serum.

By MedGene in Slovakia.

CAV3
Specificity
100 %
Genes
7 %
Muscular dystrophy, limb-girdle 1C.

By MedGene in Slovakia.

CAV3
Specificity
100 %
Genes
7 %
Rippling muscle disease.

By MedGene in Slovakia.

CAV3
Specificity
100 %
Genes
7 %
Invitae Comprehensive Neuromuscular Disorders Panel.

By Invitae in United States.

VMA21, STIM1, GMPPB, LMOD3, STAC3, POMK, TNPO3, KLHL41, MYL2, MYPN, FKBP14, LAMP2, ITGA7, B3GALNT2, COL6A1, LARGE1, COL6A3, RXYLT1, COL6A2, CHKB , (...)

View the complete list with 84 more genes
Specificity
1 %
Genes
7 %
Invitae Comprehensive Muscular Dystrophy Panel.

By Invitae in United States.

GMPPB, POMK, TNPO3, ITGA7, B3GALNT2, COL6A1, LARGE1, COL6A3, RXYLT1, COL6A2, CHKB, POMGNT2, DPM2, B4GAT1, LAMA2, ISPD, SGCD, TCAP, POMT1, POMT2 , (...)

View the complete list with 26 more genes
Specificity
3 %
Genes
7 %
Invitae Distal Myopathy Panel.

By Invitae in United States.

DNAJB6, FHL1, BAG3, MATR3, LDB3, TIA1, MYOT, ANO5, FLNC, MYH7, DES, TTN, DYSF, CAV3, SQSTM1, VCP, CRYAB, GNE
Specificity
6 %
Genes
7 %
Invitae Hypertrophic Cardiomyopathy Panel.

By Invitae in United States.

VCL, MYL3, MYL2, CSRP3, ACTN2, TNNT2, TPM1, PLN, PRKAG2, TNNI3, TNNC1, ACTC1, LAMP2, CACNA1C, TCAP, MYBPC3, FHL1, BAG3, FLNC, MYH7 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
7 %
Limb-girdle muscular dystrophy type 1C (LGMD 1C): CAV3 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

CAV3
Specificity
100 %
Genes
7 %
Rippling muscle disease: CAV3 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

CAV3
Specificity
100 %
Genes
7 %
CARDIOMYOPATHY HYPERTROPHIC PANEL.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

VCL, MYL3, MYL2, CSRP3, ACTN2, MYOZ2, JPH2, TNNT2, TPM1, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, ACTC1, PDLIM3, RYR2, LAMP2, TCAP , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
7 %
LIMB-GIRDLE MUSCULAR DYSTROPHY.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

SGCD, TCAP, POMT1, POMT2, PLEC, DAG1, DNAJB6, MYOT, ANO5, DES, TTN, DYSF, CAV3, FKRP, LMNA, CAPN3, SGCG, POMGNT1, SGCB, SGCA , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
7 %
Limb-Girdle Muscular Dystrophy Type 1C: CAV3 Gene Deletion/Duplication.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

CAV3
Specificity
100 %
Genes
7 %
Expanded Neuromuscular Disorders: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

AMPD3, MTMR14, TNNI2, GLE1, AMPD1, PLEKHG5, RYR2, CHRNG, ITGA7, COL6A1, LARGE1, COL6A3, COL6A2, LAMA2, SIL1, CHRNB1, CHRND, CHRNA1, MUSK, COLQ , (...)

View the complete list with 58 more genes
Specificity
2 %
Genes
7 %
Expanded Neuromuscular Disorders: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

MTMR14, TNNI2, GLE1, AMPD1, PLEKHG5, RYR2, CHRNG, ITGA7, COL6A1, LARGE1, COL6A3, COL6A2, LAMA2, SIL1, CHRNB1, CHRND, CHRNA1, MUSK, COLQ, ISPD , (...)

View the complete list with 57 more genes
Specificity
2 %
Genes
7 %
Neuromuscular NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

AMPD3, TNNI2, AMPD1, RYR2, PEX5, PEX12, PEX26, PEX3, PEX14, PEX6, ITGA7, COL6A1, LARGE1, COL6A3, COL6A2, LAMA2, SIL1, SGCD, TCAP, POMT1 , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
7 %
Limb-Girdle Muscular Dystrophy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

ISPD, SGCD, TCAP, DNAJB6, MYOT, ANO5, DES, TTN, DYSF, CAV3, FKRP, LMNA, CAPN3, SGCG, SGCB, SGCA, PNPLA2, TRIM32
Specificity
6 %
Genes
7 %
Distal Hereditary Myopathy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

TCAP, FHL1, MATR3, LDB3, ANO5, FLNC, MYH7, DES, TTN, DYSF, CAV3, VCP, CRYAB, GNE
Specificity
8 %
Genes
7 %
Dilated Cardiomyopathy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

VCL, DSC2, CSRP3, ACTN2, RBM20, TNNT2, TPM1, DSG2, NEXN, PLN, MYH6, TNNI3, TNNC1, ANKRD1, LAMA4, ACTC1, PKP2, ABCC9, LAMP2, SGCD , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
7 %
LGMD and Congenital Muscular Dystrophy Panel.

By Blueprint Genetics in Finland.

VMA21, COL4A2, POGLUT1, GMPPB, SPEG, TOR1AIP1, TNPO3, LIMS2, COL4A1, ITGA7, B3GALNT2, LARGE1, POMGNT2, LAMA2, SMCHD1, ISPD, SGCD, TCAP, POMT1, DNAJB6 , (...)

View the complete list with 22 more genes
Specificity
3 %
Genes
7 %
Comprehensive Muscular Dystrophy / Myopathy Panel.

By Blueprint Genetics in Finland.

TMEM126B, VMA21, COL4A2, RBCK1, POGLUT1, MICU1, GMPPB, LMOD3, SPEG, TOR1AIP1, TNPO3, LIMS2, KLHL41, COL12A1, MME, VPS13A, COL4A1, ITGA7, B3GALNT2, COL6A1 , (...)

View the complete list with 53 more genes
Specificity
2 %
Genes
7 %
Hypertrophic Cardiomyopathy NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

CALR3, VCL, MYL3, MYL2, CSRP3, ACTN2, MYOZ2, TNNT2, TPM1, MYPN, NEXN, PLN, PRKAG2, MYH6, TNNI3, TNNC1, MYLK2, ACTC1, TCAP, MYBPC3 , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
7 %
CAV3 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

CAV3
Specificity
100 %
Genes
7 %
Hypertrophic Cardiomyopathy Panel.

By ApolloGen, Inc. in United States.

MT-TQ, MT-TI, MT-TG, MYL3, MYL2, TNNT2, TPM1, PRKAG2, TNNI3, TNNC1, BMPR2, LAMP2, MYBPC3, MYH7, CAV3, MT-TK, GLA, TTR
Specificity
6 %
Genes
7 %
CAV3 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

CAV3
Specificity
100 %
Genes
7 %
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1C (AUTOSOMAL DOMINANT) (CAVEOLIN-3 DEFICIENCY).

By Laboratorio de Genetica Clinica SL in Spain.

CAV3
Specificity
100 %
Genes
7 %
Limb-Girdle Muscular Dystrophy Type 1C, Sequencing CAV3 Gene.

By Reference Laboratory Genetics in Spain.

CAV3
Specificity
100 %
Genes
7 %
Autosomal Dominant Limb-Girdle Muscular Dystrophy, Panel Massive Sequencing (NGS) 3 Genes.

By Reference Laboratory Genetics in Spain.

MYOT, CAV3, LMNA
Specificity
34 %
Genes
7 %
Phosphorus Hypertrophic Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, ACTN2, TNNT2, TPM1, PLN, PRKAG2, TNNI3, TNNC1, ACTC1, A2ML1, RRAS, SPRED1, LAMP2, RASA1, CACNA1C, TCAP, FHL1, BAG3, LDB3, FLNC , (...)

View the complete list with 29 more genes
Specificity
3 %
Genes
7 %
Phosphorus Hypertrophic Cardiomyopathy Panel.

By Phosphorus Diagnostics LLC in United States.

VCL, MYL3, MYL2, CSRP3, ACTN2, TNNT2, TPM1, PLN, PRKAG2, TNNI3, TNNC1, ACTC1, LAMP2, CACNA1C, TCAP, MYBPC3, FHL1, BAG3, LDB3, FLNC , (...)

View the complete list with 7 more genes
Specificity
4 %
Genes
7 %
Autism Spectrum Disorders 53-Gene Panel.

By Center for Human Genetics, Inc in United States.

CNTNAP5, DLGAP2, DPP10, DPP6, GRPR, PCDH9, SLC9A9, ASTN2, CADM1, CNTN4, CXCR3, FABP5, FABP7, FBXO40, GLRA2, HNRNPH2, MBD1, MBD3, MBD4, MDGA2 , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
7 %
NOS1AP.

By Institute for Human Genetics University Clinic Freiburg in Germany.

NOS1AP
Specificity
100 %
Genes
7 %
NOS1AP.

By Fulgent Genetics Fulgent Genetics in United States.

NOS1AP
Specificity
100 %
Genes
7 %
Amiodarone response.

By Xcode Life Xcode Life in India.

CYP3A4, NOS1AP
Specificity
50 %
Genes
7 %
Catecholaminergic Polymorphic Ventricular Tachycardia.

By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.

CASQ2, TRDN, CALM1, RYR2, ANK2, KCNJ2
Specificity
50 %
Genes
19 %
Catecholminergic Polymorphic Ventricular Tachycardia (CPVT) Panel.

By Cincinnati Children's Hospital Medical Center Laboratory of Genetics and Genomics Cincinnati Children's Hospital Medical Center in United States.

CASQ2, TRDN, CALM1, RYR2, ANK2, KCNJ2
Specificity
50 %
Genes
19 %
CPVTNext.

By Ambry Genetics in United States.

CASQ2, TRDN, CALM1, RYR2, ANK2, KCNJ2
Specificity
50 %
Genes
19 %
Autism Spectrum Disorders Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

MBD6, WDFY3, DGAT2L6, CDC42BPB, SYN2, STXBP5, KAT2B, TNRC6B, TCF20, KMT5B, MYO9B, CSMD1, NAA15, DSCAM, DISC1, EFR3A, CTTNBP2, CNTN6, CTNND2, ASH1L , (...)

View the complete list with 87 more genes
Specificity
1 %
Genes
7 %
Long QT syndrome type 4.

By Centogene AG - the Rare Disease Company in Germany.

ANK2
Specificity
100 %
Genes
7 %
Long QT Syndrome 4.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

ANK2
Specificity
100 %
Genes
7 %
ANK2 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

ANK2
Specificity
100 %
Genes
7 %
Long QT Syndrome Type 4 , Sequencing ANK2 Gene.

By Reference Laboratory Genetics in Spain.

ANK2
Specificity
100 %
Genes
7 %
ANK2.

By Institute for Human Genetics University Clinic Freiburg in Germany.

ANK2
Specificity
100 %
Genes
7 %
ANK2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

ANK2
Specificity
100 %
Genes
7 %
Long QT syndrome 4 (LQT4, sequence analysis of ANK2 gene).

By CGC Genetics in Portugal.

ANK2
Specificity
100 %
Genes
7 %
Long QT Syndrome via the ANK2 Gene.

By PreventionGenetics PreventionGenetics in United States.

ANK2
Specificity
100 %
Genes
7 %
Catecholaminergic Polymorphic Ventricular Tachycardia.

By Asper Biogene Asper Biogene LLC in Estonia.

CASQ2, TRDN, CALM1, RYR2, ANK2, KCNJ2
Specificity
50 %
Genes
19 %
ANK2.

By Fulgent Genetics Fulgent Genetics in United States.

ANK2
Specificity
100 %
Genes
7 %
Long QT syndrome type IV.

By Bioarray in Spain.

ANK2
Specificity
100 %
Genes
7 %
Catecholaminergic Polymorphic Ventricular Tachycardia.

By Genomics and Pathology Services Washington University in St. Louis in United States.

CASQ2, CALM1, RYR2, ANK2, KCNJ2
Specificity
40 %
Genes
13 %
ANK2 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

ANK2
Specificity
100 %
Genes
7 %
KCNH2.

By Institute for Human Genetics University Clinic Freiburg in Germany.

KCNH2
Specificity
100 %
Genes
7 %
KCNH2 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

KCNH2
Specificity
100 %
Genes
7 %
Long QT Syndrome via the KCNH2 Gene.

By PreventionGenetics PreventionGenetics in United States.

KCNH2
Specificity
100 %
Genes
7 %
QT syndrome, KCNH2.

By GGA - Galil Genetic Analysis in Israel.

KCNH2
Specificity
100 %
Genes
7 %
Long QT Syndrome 2.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

KCNH2
Specificity
100 %
Genes
7 %
Short QT Syndrome 1.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

KCNH2
Specificity
100 %
Genes
7 %
KCNH2 gene sequencing.

By Health in Code in Spain.

KCNH2
Specificity
100 %
Genes
7 %
Long QT Syndrome 2.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

KCNH2
Specificity
100 %
Genes
7 %
Long QT syndrome 2.

By Praxis fuer Humangenetik Wien in Austria.

KCNH2
Specificity
100 %
Genes
7 %
Long QT syndrome 2.

By MedGene in Slovakia.

KCNH2
Specificity
100 %
Genes
7 %
Short QT syndrome-1.

By MedGene in Slovakia.

KCNH2
Specificity
100 %
Genes
7 %
Invitae Epilepsy Panel.

By Invitae in United States.

ITPA, SNX27, FRRS1L, NGLY1, GLRA1, C12orf57, PACS1, IER3IP1, SATB2, ZDHHC9, EHMT1, ZEB2, CASK, SYN1, ARHGEF9, IQSEC2, ATRX, SERPINI1, CNTNAP2, TCF4 , (...)

View the complete list with 105 more genes
Specificity
1 %
Genes
7 %
Long QT syndrome type 2: KCNH2 gene sequence analysis.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

KCNH2
Specificity
100 %
Genes
7 %
KCNH2.

By Fulgent Genetics Fulgent Genetics in United States.

KCNH2
Specificity
100 %
Genes
7 %
Long QT syndrome type II.

By Bioarray in Spain.

KCNH2
Specificity
100 %
Genes
7 %
KCNH2 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

KCNH2
Specificity
100 %
Genes
7 %
Short QT Syndrome Type 1 , Sequencing KCNH2 Gene.

By Reference Laboratory Genetics in Spain.

KCNH2
Specificity
100 %
Genes
7 %
Long QT Syndrome Type 2 , Sequencing KCNH2 Gene.

By Reference Laboratory Genetics in Spain.

KCNH2
Specificity
100 %
Genes
7 %
Long QT syndrome 2.

By Labor Dr. Wisplinghoff in Germany.

KCNH2
Specificity
100 %
Genes
7 %
KCNH2. Complete sequencing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

KCNH2
Specificity
100 %
Genes
7 %
KCNH2. MLPA testing.

By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.

KCNH2
Specificity
100 %
Genes
7 %
Long QT Syndrome 2 (sequence analysis of KCNH2 gene).

By CGC Genetics in Portugal.

KCNH2
Specificity
100 %
Genes
7 %
Short QT syndrome 3 (deletion/duplication analysis on KCNJ2 gene).

By CGC Genetics in Portugal.

KCNH2
Specificity
100 %
Genes
7 %
Long QT syndrome type 2.

By Centogene AG - the Rare Disease Company in Germany.

KCNH2
Specificity
100 %
Genes
7 %
Short QT syndrome type 1.

By Centogene AG - the Rare Disease Company in Germany.

KCNH2
Specificity
100 %
Genes
7 %
Short QT Syndrome.

By Asper Biogene Asper Biogene LLC in Estonia.

KCNQ1-AS1, CACNB2, CACNA1C, KCNH2, KCNJ2
Specificity
20 %
Genes
7 %
Long QT syndrome, KCNH2 sequencing.

By Molecular Diagnostics Laboratory Seoul National University Hospital in South Korea.

KCNH2
Specificity
100 %
Genes
7 %
Short QT Syndrome 1.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

KCNH2
Specificity
100 %
Genes
7 %
Short QT syndrome-1.

By Praxis fuer Humangenetik Wien in Austria.

KCNH2
Specificity
100 %
Genes
7 %
Long QT syndrome type II.

By Bioarray in Spain.

KCNH2
Specificity
100 %
Genes
7 %
KCNH2 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

KCNH2
Specificity
100 %
Genes
7 %
SHORT QT SYNDROME.

By Laboratorio de Genetica Clinica SL in Spain.

KCNQ1-AS1, KCNH2
Specificity
50 %
Genes
7 %
Catecholaminergic Polymoprhic Ventricular Tachycardia.

By Molecular Cardiology Laboratories Istituti Clinici Scientifici Maugeri, IRCCS in Italy.

CASQ2, TRDN, CALM1, RYR2
Specificity
50 %
Genes
13 %
CALM1 mutation analysis.

By Laboratory of genome diagnostics Academic Medical Center, University of Amsterdam in Netherlands.

CALM1
Specificity
100 %
Genes
7 %
Catecholaminergic Polymorphic Ventricular Tachycardia and Long QT Syndrome via CALM1 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

CALM1
Specificity
100 %
Genes
7 %
Ventricular tachycardia, catecholaminergic polymorphic type 4.

By Centogene AG - the Rare Disease Company in Germany.

CALM1
Specificity
100 %
Genes
7 %
CALM1.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

CALM1
Specificity
100 %
Genes
7 %
Catecholaminergic polymorphic ventricular tachycardia.

By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.

CASQ2, TRDN, CALM1, RYR2, KCNJ2
Specificity
40 %
Genes
13 %
Catecholaminergic Polymorphic Ventricular Tachycardia NGS and Deletion/Duplication Panel.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

CALM3, CASQ2, TRDN, CALM1, RYR2, KCNJ2
Specificity
34 %
Genes
13 %
CALM1 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

CALM1
Specificity
100 %
Genes
7 %
CALM1 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

CALM1
Specificity
100 %
Genes
7 %
CALM1.

By Institute for Human Genetics University Clinic Freiburg in Germany.

CALM1
Specificity
100 %
Genes
7 %
Ventricular tachycardia, catecholaminergic polymorphic 4 (sequence analysis of CALM1 gene).

By CGC Genetics in Portugal.

CALM1
Specificity
100 %
Genes
7 %
CALM1.

By Fulgent Genetics Fulgent Genetics in United States.

CALM1
Specificity
100 %
Genes
7 %
Malformations of Cortical Development.

By MGZ Medical Genetics Center in Germany.

DSC2, JUP, DSG2, TGFB3, TRDN, RYR2, PKP2, EFHC1, TMEM43, DES, FGFR3, DSP
Specificity
9 %
Genes
7 %
Ventricular tachycardia, catecholaminergic polymorphic type 5.

By Centogene AG - the Rare Disease Company in Germany.

TRDN
Specificity
100 %
Genes
7 %
qCarrier Plus.

By Quantitative Genomic Medicine Laboratories, SL in Spain.

MPP3, FTCD, ADK, CTH, HAL, HGD, WNT10A, SLC6A19, TPO, SLC5A5, DUOX2, DUOXA2, PAX8, HJV, HOGA1, TFR2, COL7A1, SLC39A4, ARL13B, FANCA , (...)

View the complete list with 280 more genes
Specificity
1 %
Genes
7 %
TRDN Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

TRDN
Specificity
100 %
Genes
7 %
TRDN Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

TRDN
Specificity
100 %
Genes
7 %
TRDN.

By Institute for Human Genetics University Clinic Freiburg in Germany.

TRDN
Specificity
100 %
Genes
7 %
Catecholaminergic Polymorphic Ventricular Tachycardia via the TRDN Gene.

By PreventionGenetics PreventionGenetics in United States.

TRDN
Specificity
100 %
Genes
7 %
TRDN.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

TRDN
Specificity
100 %
Genes
7 %
TRDN.

By Fulgent Genetics Fulgent Genetics in United States.

TRDN
Specificity
100 %
Genes
7 %
Long QT syndrome 12 (sequence analysis of SNTA1 gene).

By CGC Genetics in Portugal.

SNTA1
Specificity
100 %
Genes
7 %
SNTA1 Gene Sequencing and Deletion/Duplication Analysis.

By DDC Clinic Molecular Diagnostics Laboratory DDC Clinic, Center for Special Needs Children in United States.

SNTA1
Specificity
100 %
Genes
7 %
SNTA1 Gene, entire coding region or targeted variant.

By Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease Montreal Heart Institute in Canada.

SNTA1
Specificity
100 %
Genes
7 %
SNTA1.

By Institute for Human Genetics University Clinic Freiburg in Germany.

SNTA1
Specificity
100 %
Genes
7 %
Long QT syndrome via the SNTA1 Gene.

By PreventionGenetics PreventionGenetics in United States.

SNTA1
Specificity
100 %
Genes
7 %
Long QT syndrome type 12.

By Centogene AG - the Rare Disease Company in Germany.

SNTA1
Specificity
100 %
Genes
7 %
Long QT Syndrome 12.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SNTA1
Specificity
100 %
Genes
7 %
SNTA1.

By Fulgent Genetics Fulgent Genetics in United States.

SNTA1
Specificity
100 %
Genes
7 %
Long QT syndrome type XII.

By Bioarray in Spain.

SNTA1
Specificity
100 %
Genes
7 %

Alternate names

Long Qt Syndrome 5; Lqt5 Is also known as ;romano-ward long qt syndrome.



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