Atrial Standstill 1; Atrst1

Description

Atrial standstill (AS) is a rare condition characterized by the absence of electrical and mechanical activity in the atria. On surface ECG, AS is distinguished by bradycardia, junctional (usually narrow complex) escape rhythm, and absence of the P wave. Nearly 50% of patients with AS experience syncope. AS can be persistent or transient, and diffuse or partial (summary by Fazelifar et al., 2005).

Clinical Features

Top most frequent phenotypes and symptoms related to Atrial Standstill 1; Atrst1

  • Milia
  • Congestive heart failure
  • Bradycardia
  • Atrial fibrillation
  • Amyloidosis
  • Heart block
  • Paroxysmal atrial fibrillation
  • Endocardial fibroelastosis
  • Sick sinus syndrome
  • Premature atrial contractions
And another 4 symptoms. If you need more information about this disease we can help you.
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Incidence and onset information

Not enough data available about incidence and published cases.


Mendelian

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Atrial Standstill 1; Atrst1 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Epilepsy Advanced Sequencing and CNV Evaluation - Generalized, Absence, Focal,Febrile and Myoclonic Epilepsies.

By Athena Diagnostics Inc in United States.

ALPL, ADSL, SLC25A19, LIAS, ABAT, GAMT, GATM, SUCLA2, ALG9, GLDC, AMT, ALDH7A1, NDUFA1, L2HGDH, CYP27A1, SLC6A8, CHRNA7, PCDH19, SLC2A1, PHGDH , (...)

View the complete list with 64 more genes
Specificity
2 %
Genes
34 %
Epilepsy Advanced Sequencing and CNV Evaluation.

By Athena Diagnostics Inc in United States.

UBE3A, ALPL, ADSL, PAX6, CPT2, ATP6V0A2, HSD17B10, HPRT1, ADGRV1, SHH, POLG, SLC25A19, PANK2, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, SUCLA2 , (...)

View the complete list with 214 more genes
Specificity
1 %
Genes
34 %
NGS Epilepsy/Seizure Panel.

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

MTHFR, UBE3A, ADSL, SHH, POLG, SLC25A19, MECP2, LIAS, ABAT, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH7A1, NDUFA1, TPP1, CLN3, ARX , (...)

View the complete list with 125 more genes
Specificity
1 %
Genes
34 %
Brugada Syndrome Panel.

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

KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA1C, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2
Specificity
7 %
Genes
34 %
Long QT Syndrome Panel.

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

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, CASQ2, AKAP9, SCN4B
Specificity
6 %
Genes
34 %
Comprehensive Cardiac Panel.

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

TTR, AGL, ACADVL, GAA, DSP, CRYAB, RAF1, MTO1, TMEM70, TAZ, SLC22A5, ALMS1, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS , (...)

View the complete list with 87 more genes
Specificity
1 %
Genes
34 %
Dilated & Arrhythmogenic Cardiomyopathies Panel.

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

TTR, DSP, CRYAB, RAF1, TAZ, DOLK, DMD, GLA, PTPN11, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, TMEM43, EMD, TCAP, SGCD , (...)

View the complete list with 31 more genes
Specificity
2 %
Genes
34 %
Cardiomyopathy Panel.

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

TTR, GAA, COL3A1, EYA4, DSP, CRYAB, RAF1, FBN1, SCO2, TAZ, COX15, SURF1, CBS, FXN, COL5A1, COL5A2, BRAF, DMD, GLA, HRAS , (...)

View the complete list with 92 more genes
Specificity
1 %
Genes
34 %
Dilated Cardiomyopathy Panel.

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

TTR, EYA4, DSP, CRYAB, RAF1, TAZ, DMD, FKTN, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, EMD, TCAP, SGCD, SCN5A, LAMP2 , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
34 %
Brugada Syndrome.

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

SCN1B, HCN4, SCN5A, CACNA1C, TRPM4, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
12 %
Genes
34 %
Comprehensive Arrhythmias Panel.

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

CAV3, KCNJ2, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, TRPM4, SCN3B, KCNE3, CACNB2, GPD1L, ANK2, RYR2, CALM1, TRDN, KCNE2, SNTA1 , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
34 %
Long QT Syndrome and Short QT Syndrome.

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

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, KCNE2, SNTA1, AKAP9, SCN4B
Specificity
8 %
Genes
34 %
Atrioventricular Block Panel.

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

LMNA, DES, EMD, SCN1B, SCN5A, TRPM4, NKX2-5
Specificity
15 %
Genes
34 %
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.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B
Specificity
8 %
Genes
34 %
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.

CRYAB, TAZ, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, NEBL, ACTC1, ANKRD1, TNNC1, TNNI3 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
34 %
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.

TTR, CRYAB, SCO2, TAZ, SURF1, LMNA, CAV3, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, NEBL , (...)

View the complete list with 17 more genes
Specificity
3 %
Genes
34 %
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.

CRYAB, TAZ, DMD, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, NEBL, ACTC1, ANKRD1, TNNC1 , (...)

View the complete list with 11 more genes
Specificity
4 %
Genes
34 %
Atrial Fibrillation Panel.

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

LMNA, KCNJ2, KCND3, KCNH2, SCN1B, SCN5A, KCNE1, KCNQ1, ABCC9, SCN2B, SCN3B, KCNE2, KCNA5, NUP155, NPPA, GJA5
Specificity
19 %
Genes
100 %
Brugada Syndrome Panel.

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

KCND3, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1C, TRPM4, SLMAP, KCNJ8, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, RANGRF
Specificity
7 %
Genes
34 %
Cardiac Channelopathy Panel.

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

CAV3, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
34 %
LQTS panel.

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

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, CALM2, KCNE2, AKAP9, SCN4B
Specificity
8 %
Genes
34 %
Targeted CM panel.

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

DSP, LMNA, MYH7, LDB3, MYBPC3, TMEM43, SCN5A, PKP2, TNNI3, NEXN, DSG2, JUP, TPM1, TNNT2, DSC2
Specificity
7 %
Genes
34 %
Cardiac Arrhythmia Gene Panel.

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

DSP, GLA, LMNA, MYH7, BAG3, MYBPC3, KCNJ2, KCNH2, SCN1B, SCN5A, KCNE1, KCNQ1, CACNA1C, CACNB2, PKP2, RYR2, KCNE2, CASQ2, KCNA5, TNNI3 , (...)

View the complete list with 8 more genes
Specificity
4 %
Genes
34 %
SCN5A.

By Institute for Human Genetics University Clinic Freiburg in Germany.

SCN5A
Specificity
100 %
Genes
34 %
DCM/Arrhythmogenic Cardiomyopathy Panel (53 Genes).

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

TTR, DSP, CRYAB, RAF1, TAZ, DOLK, DMD, GLA, PTPN11, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, TMEM43, EMD, TCAP, SGCD , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
34 %
Pan Cardiomyopathy Panel (62 Genes).

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

TTR, DSP, CRYAB, RAF1, TAZ, DOLK, DMD, GLA, PTPN11, LMNA, CAV3, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, TMEM43, EMD, TCAP , (...)

View the complete list with 41 more genes
Specificity
2 %
Genes
34 %
Cardiomyopathy and Arrhythmia Panel, Sequencing (85 Genes) and Deletion/Duplication (83 Genes).

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

TTR, GAA, EYA4, DSP, SLC25A4, SCO2, TAZ, COX15, FXN, DMD, GLA, FKTN, SGCA, SGCB, SGCG, LMNA, FKRP, CAV3, TTN, DES , (...)

View the complete list with 65 more genes
Specificity
2 %
Genes
34 %
Brugada Syndrome Sequencing Panel.

By GeneDx in United States.

SCN1B, SCN5A, CACNA1C, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
15 %
Genes
34 %
Comprehensive Cardiomyopathy Panel.

By GeneDx in United States.

TTR, DSP, CRYAB, RAF1, TAZ, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SOS1, MAP2K2, FKTN, LMNA, MT-TL1, MT-TK, MT-ND1 , (...)

View the complete list with 56 more genes
Specificity
2 %
Genes
34 %
Comprehensive Arrhythmia Panel.

By GeneDx in United States.

DSP, CAV3, TMEM43, KCNJ2, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, KCNJ8, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, KCNE2 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
34 %
DCM/LVNC Sequencing Panel.

By GeneDx in United States.

TTR, TAZ, LMNA, MT-TK, MT-ND1, MT-ND6, TTN, DES, MYH7, LDB3, MYBPC3, EMD, TCAP, SGCD, SCN5A, MT-TS1, MT-TS2, LAMP2, ACTC1, ANKRD1 , (...)

View the complete list with 17 more genes
Specificity
3 %
Genes
34 %
Long QT Syndrome Gene Sequencing & Del/Dup Panel.

By GeneDx in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, KCNE2, SNTA1, AKAP9, SCN4B
Specificity
9 %
Genes
34 %
Long QT Syndrome Sequencing Panel.

By GeneDx in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, KCNE2, SNTA1, AKAP9, SCN4B
Specificity
9 %
Genes
34 %
Long QT Syndrome Del/Dup Panel.

By GeneDx in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, KCNE2, SNTA1, AKAP9, SCN4B
Specificity
9 %
Genes
34 %
CardioNext with TTN.

By Ambry Genetics in United States.

TTR, EYA4, JAG1, DSP, CRYAB, RAF1, TAZ, FXN, DMD, GLA, PTPN11, FKTN, LMNA, CAV3, TTN, DES, MYH7, LDB3, BAG3, MYBPC3 , (...)

View the complete list with 65 more genes
Specificity
2 %
Genes
34 %
CMNext with TTN.

By Ambry Genetics in United States.

TTR, EYA4, DSP, CRYAB, RAF1, TAZ, FXN, DMD, GLA, PTPN11, FKTN, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, TMEM43, EMD , (...)

View the complete list with 35 more genes
Specificity
2 %
Genes
34 %
CustomNext: Cardio.

By Ambry Genetics in United States.

TTR, COL3A1, EYA4, JAG1, DSP, CRYAB, RAF1, FBN1, TAZ, CBS, FXN, COL5A1, COL5A2, DMD, GLA, PLOD1, PTPN11, SMAD4, FKTN, LMNA , (...)

View the complete list with 86 more genes
Specificity
1 %
Genes
34 %
DCMNext with TTN.

By Ambry Genetics in United States.

TTR, EYA4, RAF1, TAZ, DMD, FKTN, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, TCAP, SCN5A, LAMP2, ABCC9, ACTC1, LAMA4, NKX2-5 , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
34 %
RhythmNext.

By Ambry Genetics in United States.

DSP, LMNA, CAV3, TMEM43, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, TRPM4, KCNJ8, SCN3B, KCNE3, CACNB2, GPD1L , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
34 %
RhythmFirst.

By Ambry Genetics in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, KCNE2, SNTA1, AKAP9, SCN4B
Specificity
9 %
Genes
34 %
RhythmFirst reflex RhythmNext.

By Ambry Genetics in United States.

DSP, LMNA, CAV3, TMEM43, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, TRPM4, KCNJ8, SCN3B, KCNE3, CACNB2, GPD1L , (...)

View the complete list with 16 more genes
Specificity
3 %
Genes
34 %
SCN5A mutation analysis.

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

SCN5A
Specificity
100 %
Genes
34 %
Cardiomyopathy NGS Multi-Gene Panel (50 genes), Sequence & CNV analysis.

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

TTR, DSP, CRYAB, TAZ, GLA, LMNA, CAV3, TTN, DES, MYH7, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, HCN4, SCN5A , (...)

View the complete list with 31 more genes
Specificity
2 %
Genes
34 %
LQT Multi-Gene Package.

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

KCNH2, SCN5A, KCNE1, KCNQ1, KCNE2
Specificity
20 %
Genes
34 %
Cardiac Arrhythmia NGS Multi-Gene Panel (48 genes), Sequence & CNV analysis.

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

LMNA, CAV3, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1D, KCNE1, KCNQ1, CACNA1C, LAMP2, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B , (...)

View the complete list with 27 more genes
Specificity
7 %
Genes
100 %
CAV3, KCNE1, KCNE2, KCNH2, KCNQ1, SCN5A. NextGeneDx.Complete sequencing by NGS.

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

CAV3, KCNH2, SCN5A, KCNE1, KCNQ1, KCNE2
Specificity
17 %
Genes
34 %
LMNA, MYBPC3, MYH7, SCN5A, TNNI3, TNNT2. NextGeneDx.Complete sequencing by NGS.

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

LMNA, MYH7, MYBPC3, SCN5A, TNNI3, TNNT2
Specificity
17 %
Genes
34 %
SCN5A. Complete sequencing.

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

SCN5A
Specificity
100 %
Genes
34 %
SCN5A. Complete sequencing.

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

SCN5A
Specificity
100 %
Genes
34 %
KCNH2, KCNQ1, SCN5A. NextGeneDx.Complete sequencing by NGS.

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

KCNH2, SCN5A, KCNQ1
Specificity
34 %
Genes
34 %
SCN5A-Related Dilated Cardiomyopathy.

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
34 %
Long QT syndrome 3 (sequence analysis of SCN5A gene).

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
34 %
SCN5A-Related Disorders.

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
34 %
Brugada Syndrome 1 (sequence analysis of SCN5A gene).

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
34 %
Brugada syndrome (NGS panel for 7 genes).

By CGC Genetics in Portugal.

SCN1B, SCN5A, CACNA1C, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
15 %
Genes
34 %
Cardiac conduction changes (NGS panel for 27 genes).

By CGC Genetics in Portugal.

CAV3, KCNJ2, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, SCN3B, KCNE3, CACNB2, GPD1L, ANK2, RYR2, CALM1, TRDN, KCNE2, KCNJ5, SNTA1 , (...)

View the complete list with 7 more genes
Specificity
4 %
Genes
34 %
Long QT syndrome (NGS panel for 14 genes).

By CGC Genetics in Portugal.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B, ALG10
Specificity
8 %
Genes
34 %
Cardiomyopathy and changes in cardiac conduction (NGS panel for 59 genes).

By CGC Genetics in Portugal.

DSP, GLA, LMNA, CAV3, TTN, DES, MYH7, LDB3, MYBPC3, TMEM43, TCAP, SGCD, KCNJ2, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C , (...)

View the complete list with 39 more genes
Specificity
2 %
Genes
34 %
Sinus node syndrome (NGS panel for 3 genes).

By CGC Genetics in Portugal.

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

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
34 %
Familial dilated cardiomyopathy type 1E (deletions/duplications analysis of SCN5A gene).

By CGC Genetics in Portugal.

SCN5A
Specificity
100 %
Genes
34 %
Brugada Syndrome type 1.

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

SCN5A
Specificity
100 %
Genes
34 %
Long QT syndrome.

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

KCNH2, SCN5A, KCNE1, KCNQ1, KCNE2
Specificity
20 %
Genes
34 %
Brugada Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

KCND3, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1C, TRPM4, SLMAP, KCNJ8, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, RANGRF, KCNE5
Specificity
7 %
Genes
34 %
Long QT Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, CALM2, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B
Specificity
7 %
Genes
34 %
Familial Atrial Fibrillation Syndrome Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

KCNJ2, KCND3, KCNH2, SCN1B, SCN5A, KCNE1, KCNQ1, ABCC9, SCN2B, SCN3B, KCNE2, KCNA5, NPPA, GJA5, KCNE5
Specificity
20 %
Genes
100 %
Comprehensive Cardiology Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

HFE, TTR, GAA, COL3A1, ELN, EYA4, JAG1, DSP, SLC25A4, CRYAB, HADHA, RAF1, FBN1, GCKR, DNAJC19, SCO2, TAZ, COX15, CBS, ALMS1 , (...)

View the complete list with 144 more genes
Specificity
2 %
Genes
100 %
Sudden Cardiac Arrest Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

TTR, EYA4, DSP, FBN1, NRAS, FKTN, LMNA, CAV3, DES, MYH7, MYBPC3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, TGFBR2, FBN2, ABCC9 , (...)

View the complete list with 29 more genes
Specificity
3 %
Genes
34 %
Dilated Cardiomyopathy Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

TTR, EYA4, DSP, CRYAB, RAF1, TAZ, DMD, FKTN, LMNA, CAV3, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, EMD, TCAP, SGCD, SCN5A , (...)

View the complete list with 27 more genes
Specificity
3 %
Genes
34 %
Pan Cardiomyopathy Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

TTR, GAA, EYA4, DSP, CRYAB, RAF1, SCO2, TAZ, ALMS1, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SOS1, MAP2K2 , (...)

View the complete list with 62 more genes
Specificity
2 %
Genes
34 %
Catecholaminergic Polymorphic Ventricular Tachycardia Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

KCNJ2, SCN5A, KCNQ1, ANK2, RYR2, CALM1, TRDN, CASQ2
Specificity
13 %
Genes
34 %
Brugada Syndrome 1 via the SCN5A Gene.

By PreventionGenetics PreventionGenetics in United States.

SCN5A
Specificity
100 %
Genes
34 %
Fetal Concerns Sequencing Panel Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

GNPTAB, GLB1, RAF1, CTSA, GUSB, GALNS, GBA, BRAF, DHCR7, HRAS, IDUA, KRAS, LIPA, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, RIT1, MAP2K2 , (...)

View the complete list with 20 more genes
Specificity
3 %
Genes
34 %
Comprehensive Cardiac Arrhythmia Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

DSP, CAV3, DES, LDB3, TMEM43, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B , (...)

View the complete list with 35 more genes
Specificity
6 %
Genes
100 %
Epilepsy and Seizure Plus Sequencing Panel with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

UBE3A, PTEN, ADSL, POLG, MECP2, LIAS, DHDDS, ABAT, SLC25A12, GAMT, GATM, STXBP1, CTSD, SLC25A22, GCSH, GLDC, AMT, SLC9A6, ALDH5A1, ALDH7A1 , (...)

View the complete list with 202 more genes
Specificity
1 %
Genes
34 %
Atrioventricular block Deletion/ Duplication panel.

By Connective Tissue Gene Tests in United States.

LMNA, DES, EMD, SCN1B, SCN5A, TRPM4, NKX2-5
Specificity
15 %
Genes
34 %
Brugada syndrome and related disorders Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

GAA, GLA, CAV3, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1C, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
34 %
Brugada syndrome and related disorders NGS panel.

By Connective Tissue Gene Tests in United States.

GAA, GLA, CAV3, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1C, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
34 %
Cardiac channelopathy Deletion/ Duplication panel.

By Connective Tissue Gene Tests in United States.

CAV3, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L , (...)

View the complete list with 21 more genes
Specificity
3 %
Genes
34 %
Brugada syndrome and related disorders Comprehensive panel.

By Connective Tissue Gene Tests in United States.

GAA, GLA, CAV3, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1C, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
34 %
Cardiac channelopathy Comprehensive panel.

By Connective Tissue Gene Tests in United States.

CAV3, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L , (...)

View the complete list with 21 more genes
Specificity
3 %
Genes
34 %
Cardiac channelopathy NGS panel.

By Connective Tissue Gene Tests in United States.

CAV3, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L , (...)

View the complete list with 21 more genes
Specificity
3 %
Genes
34 %
Long QT syndrome Comprehensive panel.

By Connective Tissue Gene Tests in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B, NOS1AP, CALM3
Specificity
6 %
Genes
34 %
Long QT syndrome NGS panel.

By Connective Tissue Gene Tests in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B, NOS1AP, CALM3
Specificity
6 %
Genes
34 %
Long QT syndrome Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B, NOS1AP, CALM3
Specificity
6 %
Genes
34 %
Progressive familial heart block type I NGS panel.

By Connective Tissue Gene Tests in United States.

SCN5A, TRPM4
Specificity
50 %
Genes
34 %
Progressive familial heart block type I Comprehensive panel.

By Connective Tissue Gene Tests in United States.

SCN5A, TRPM4
Specificity
50 %
Genes
34 %
Progressive familial heart block type I Deletion / Duplication panel.

By Connective Tissue Gene Tests in United States.

SCN5A, TRPM4
Specificity
50 %
Genes
34 %
Brugada Syndrome.

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

SCN5A
Specificity
100 %
Genes
34 %
Heart Diseases - panels.

By MGZ Medical Genetics Center in Germany.

TTR, AARS2, ACAD9, ACADM, ACADS, AGL, ACADVL, GAA, ELN, CPT2, GNE, JAG1, DSP, CRYAB, RAF1, VCP, FBN1, MTO1, AGK, TMEM70 , (...)

View the complete list with 137 more genes
Specificity
1 %
Genes
34 %
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) / Arrhythmogenic Right Ventricular Dysplasia (ARVD).

By MGZ Medical Genetics Center in Germany.

SCN5A, CALM1, CASQ2
Specificity
34 %
Genes
34 %
Dilated Cardiomyopathy Sequential Panel.

By FirmaLab in United States.

LMNA, TTN, MYH7, SCN5A, ACTC1, TNNT2
Specificity
17 %
Genes
34 %
Brugada Syndrome 1.

By Bioscientia GmbH Center for Human Genetics in Germany.

SCN5A
Specificity
100 %
Genes
34 %
SCN5A-Related Disorders.

By Bioscientia GmbH Center for Human Genetics in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Long QT syndrome.

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

KCNH2, SCN5A, KCNE1, KCNQ1, KCNE2
Specificity
20 %
Genes
34 %
Brugada syndrome.

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

SCN5A
Specificity
100 %
Genes
34 %
Cardiac conduction abnormalities panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

DSP, LMNA, CAV3, CACNA1A, DES, TMEM43, KCNJ2, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, KCNJ8, SCN3B, KCNE3, CACNB2, GPD1L, PKP2 , (...)

View the complete list with 13 more genes
Specificity
4 %
Genes
34 %
Cardiomyopathy panel.

By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.

TTR, EYA4, DSP, CRYAB, TAZ, DMD, GLA, FKTN, LMNA, CAV3, DES, MYH7, FLNC, MYOT, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD , (...)

View the complete list with 41 more genes
Specificity
2 %
Genes
34 %
Long QT syndrome type 3.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Sick sinus syndrome.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Ventricular fibrillation, paroxysmal familial type 1.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Brugada syndrome panel.

By Centogene AG - the Rare Disease Company in Germany.

SCN1B, HCN4, SCN5A, CACNA1C, SLMAP, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
12 %
Genes
34 %
Long QT syndrome panel.

By Centogene AG - the Rare Disease Company in Germany.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B
Specificity
8 %
Genes
34 %
Atrial fibrillation type 10.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Cardiomyopathy, dilated type 1E.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Heart block type 1.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
34 %
AllNeuro panel.

By Centogene AG - the Rare Disease Company in Germany.

F2, F5, FMR1, HTT, HFE, MTHFR, TTR, UBE3A, VHL, PTEN, AARS2, ABHD12, ACACA, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1 , (...)

View the complete list with 1185 more genes
Specificity
1 %
Genes
34 %
Arrhythmia, familial panel.

By Centogene AG - the Rare Disease Company in Germany.

DSP, CAV3, TMEM43, KCNJ2, KCNH2, SCN1B, SCN5A, KCNE1, KCNQ1, CACNA1C, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, KCNE2, SNTA1, CASQ2 , (...)

View the complete list with 9 more genes
Specificity
7 %
Genes
67 %
Brugada syndrome type 1.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Sudden infant death syndrom.

By Centogene AG - the Rare Disease Company in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Brugada Syndrome Panel.

By CeGaT GmbH in Germany.

KCND3, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1C, TRPM4, KCNJ8, SCN3B, KCNE3, CACNB2, GPD1L, SCN10A
Specificity
8 %
Genes
34 %
Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT), Paroxysmal/ Idiopathic Ventricular Fibrillation / Tachycardia Panel.

By CeGaT GmbH in Germany.

KCNJ2, SCN5A, ANK2, RYR2, CALM1, CALM2, TRDN, CASQ2, DPP6, GNAI2
Specificity
10 %
Genes
34 %
Atrial Fibrillation and Short QT Syndrome Panel.

By CeGaT GmbH in Germany.

KCNJ2, KCNH2, SCN1B, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, ABCC9, SCN2B, SCN3B, CACNB2, KCNE2, SCN4B, KCNA5, NPPA, GJA5
Specificity
18 %
Genes
100 %
Long QT Syndrome Panel.

By CeGaT GmbH in Germany.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, CALM2, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B
Specificity
7 %
Genes
34 %
BRUGADA SYNDROME 1; BRGDA1.

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

SCN5A
Specificity
100 %
Genes
34 %
SCN5A sequencing.

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

SCN5A
Specificity
100 %
Genes
34 %
QT syndrome, SCN5A.

By GGA - Galil Genetic Analysis in Israel.

SCN5A
Specificity
100 %
Genes
34 %
SCN5A-Related Disorders.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Brugada Syndrome 1.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Brugada Syndrome 1.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Cardio-channelopathy-gene-panel.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

CAV3, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, TRPM4, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, ANK2, RYR2 , (...)

View the complete list with 13 more genes
Specificity
10 %
Genes
100 %
Long QT Syndrome 3.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Sick-Sinus-Syndrome 1.

By MVZ Dortmund Dr. Eberhard & Partner in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Long QT Syndrome.

By Asper Biogene Asper Biogene LLC in Estonia.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B
Specificity
8 %
Genes
34 %
Brugada Syndrome.

By Asper Biogene Asper Biogene LLC in Estonia.

KCND3, SCN1B, HCN4, SCN5A, CACNA1C, TRPM4, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
10 %
Genes
34 %
Arrhythmia.

By Asper Biogene Asper Biogene LLC in Estonia.

DSP, LMNA, CAV3, DES, TMEM43, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2 , (...)

View the complete list with 18 more genes
Specificity
8 %
Genes
100 %
Dilated Cardiomyopathy.

By Asper Biogene Asper Biogene LLC in Estonia.

TTR, EYA4, DSP, CRYAB, RAF1, TAZ, DMD, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9 , (...)

View the complete list with 22 more genes
Specificity
3 %
Genes
34 %
Long QT syndrome, SCN5A sequencing.

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

SCN5A
Specificity
100 %
Genes
34 %
SCN5A gene sequencing.

By Health in Code in Spain.

SCN5A
Specificity
100 %
Genes
34 %
Dilated cardiomyopathy with conduction disorders Stage 3.

By Health in Code in Spain.

SCN5A
Specificity
100 %
Genes
34 %
Standard Long QT syndrome Stage 1.

By Health in Code in Spain.

KCNH2, SCN5A, KCNE1, KCNQ1, KCNE2
Specificity
20 %
Genes
34 %
Long QT Syndrome Extended Panel.

By Health in Code in Spain.

CAV3, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, KCNE3, ANK2, RYR2, CALM1, CALM2, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
34 %
Auricular Fibrillation Panel.

By Health in Code in Spain.

TTR, PITX2, LMNA, EMD, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, RYR2, KCNE2 , (...)

View the complete list with 18 more genes
Specificity
8 %
Genes
100 %
J Wave Syndrome Panel.

By Health in Code in Spain.

KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1D, CACNA1C, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RANGRF , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
34 %
Inherited Cardiovascular Diseases and Sudden Death Panel.

By Health in Code in Spain.

HFE, TTR, AARS2, ACAD9, ACADM, AGL, ACADVL, ATPAF2, GAA, COL1A1, COL1A2, COL3A1, PSEN1, ELN, EYA4, GNPTAB, GLB1, PITX2, JAG1, DSP , (...)

View the complete list with 193 more genes
Specificity
2 %
Genes
100 %
Brugada Syndrome Panel.

By Health in Code in Spain.

KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1D, CACNA1C, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RANGRF , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
34 %
Dilated Cardiomyopathy Panel.

By Health in Code in Spain.

HFE, TTR, GAA, PSEN1, EYA4, GLB1, DSP, CRYAB, RAF1, DNAJC19, TAZ, SLC22A5, ALMS1, DOLK, BRAF, DMD, GLA, PTPN11, FKTN, SGCA , (...)

View the complete list with 61 more genes
Specificity
2 %
Genes
34 %
Ventricular Arrythmia & Sudden Death Panel with Structural Heart Disease.

By Health in Code in Spain.

HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATPAF2, GAA, GNPTAB, GLB1, PITX2, DSP, DLD, SLC25A4, CRYAB, RAF1, MTO1, MRPL3, LIAS, AGK , (...)

View the complete list with 121 more genes
Specificity
3 %
Genes
100 %
Catecholaminergic Polymorphic VT Panel.

By Health in Code in Spain.

KCNJ2, SCN5A, ANK2, RYR2, CALM1, CALM2, TRDN, CASQ2
Specificity
13 %
Genes
34 %
Long QT Syndrome Short Panel.

By Health in Code in Spain.

KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, RYR2, KCNE2
Specificity
13 %
Genes
34 %
Cardiac Conduction Disease Panel.

By Health in Code in Spain.

HFE, TTR, GAA, GLA, LMNA, DES, MYH7, LDB3, EMD, KCNH2, SCN1B, HCN4, SCN5A, CACNA1D, KCNQ1, LAMP2, TRPM4, KCNE2, SCN4B, ACTC1 , (...)

View the complete list with 8 more genes
Specificity
11 %
Genes
100 %
Ventricular Arrythmia & Sudden Death Panel without Structural Heart Disease.

By Health in Code in Spain.

ACADM, DSP, LMNA, CAV3, DES, FLNC, TMEM43, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1D, KCNE1, KCNQ1, CACNA1C, LAMP2, TRPM4 , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
34 %
Cardiomyopathies Panel.

By Health in Code in Spain.

HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATPAF2, GAA, PSEN1, ELN, EYA4, GNPTAB, GLB1, PITX2, JAG1, DSP, DLD, SLC25A4, CRYAB, RAF1 , (...)

View the complete list with 129 more genes
Specificity
2 %
Genes
67 %
Arrythmogenic Cardiomyopathy Panel.

By Health in Code in Spain.

DSP, LMNA, TTN, DES, FLNC, LDB3, TMEM43, SCN5A, PKP2, RYR2, CASQ2, TGFB3, PLN, DSG2, JUP, DSC2, CTNNA3
Specificity
6 %
Genes
34 %
Long QT Syndrome Extended Panel.

By Health in Code in Spain.

CAVIN1, CAV3, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, KCNE3, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1 , (...)

View the complete list with 8 more genes
Specificity
4 %
Genes
34 %
Arrhythmogenic cardiomyopathy.

By Health in Code in Spain.

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

View the complete list with 1 more genes
Specificity
5 %
Genes
34 %
Long QT Syndrome Panel.

By Health in Code in Spain.

KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, RYR2, KCNE2
Specificity
13 %
Genes
34 %
Ventricular arrhythmia and sudden death without structural heart disease.

By Health in Code in Spain.

HFE, TTR, GAA, DSP, CAVIN1, GLA, LMNA, CAV3, DES, MYH7, FLNC, LDB3, SYNE1, TMEM43, SYNE2, EMD, KCNJ2, KCND3, KCNH2, SCN1B , (...)

View the complete list with 57 more genes
Specificity
4 %
Genes
100 %
Cardiovascular Diseases_General Panel.

By Health in Code in Spain.

HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATP5F1E, ATP7A, ATPAF2, B4GALT7, GAA, HNF1A, NEUROD1, PPARG, COL1A1, COL1A2, COL3A1, ELAC2, PSEN1, HNF1B , (...)

View the complete list with 360 more genes
Specificity
1 %
Genes
100 %
Cardiac conduction disease Panel.

By Health in Code in Spain.

HFE, TTR, GAA, GLA, LMNA, DES, MYH7, LDB3, SYNE1, SYNE2, EMD, KCNJ2, KCNH2, SCN1B, HCN4, SCN5A, CACNA1D, KCNQ1, LAMP2, TRPM4 , (...)

View the complete list with 14 more genes
Specificity
9 %
Genes
100 %
Atrial fibrillation Panel.

By Health in Code in Spain.

TTR, PITX2, ZFHX3, LMNA, EMD, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, RYR2 , (...)

View the complete list with 23 more genes
Specificity
7 %
Genes
100 %
Brugada syndrome / J wave syndrome.

By Health in Code in Spain.

KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1D, CACNA1C, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RANGRF , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
34 %
Arrhythmia General Panel.

By Health in Code in Spain.

HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATP5F1E, ATPAF2, GAA, ELAC2, PSEN1, EYA4, GNPTAB, GLB1, PITX2, DSP, DLD, SLC25A4, FOXRED1, CRYAB , (...)

View the complete list with 198 more genes
Specificity
2 %
Genes
100 %
Catecholaminergic polymorphic ventricular tachycardia panel.

By Health in Code in Spain.

KCNJ2, SCN5A, ANK2, RYR2, CALM1, CALM2, TRDN, CASQ2, CALM3
Specificity
12 %
Genes
34 %
Cardiomyopathies General Panel.

By Health in Code in Spain.

HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATP5F1E, ATPAF2, GAA, ELAC2, PSEN1, EYA4, GNPTAB, GLB1, DSP, DLD, SLC25A4, FOXRED1, CRYAB, RAF1 , (...)

View the complete list with 153 more genes
Specificity
1 %
Genes
34 %
Brugada Syndrome 1.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

SCN5A
Specificity
100 %
Genes
34 %
SCN5A-Related Disorders.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

SCN5A
Specificity
100 %
Genes
34 %
Long QT Syndrome 3.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

SCN5A
Specificity
100 %
Genes
34 %
SCN5A-Related Dilated Cardiomyopathy.

By Clinical Genomics Maastricht University Medical Centre in Netherlands.

SCN5A
Specificity
100 %
Genes
34 %
SCN5A Gene Sequencing.

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

SCN5A
Specificity
100 %
Genes
34 %
Invitae Arrhythmia Comprehensive Panel.

By Invitae in United States.

DSP, LMNA, CAV3, TTN, DES, FLNC, TMEM43, EMD, KCNJ2, KCNH2, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, ABCC9, CACNB2, GPD1L, PKP2, ANK2 , (...)

View the complete list with 19 more genes
Specificity
3 %
Genes
34 %
Invitae Arrhythmia and Cardiomyopathy Comprehensive Panel.

By Invitae in United States.

TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, GLA, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC , (...)

View the complete list with 47 more genes
Specificity
2 %
Genes
34 %
Invitae Arrhythmogenic Cardiomyopathy Panel.

By Invitae in United States.

DSP, LMNA, TTN, DES, FLNC, TMEM43, EMD, SCN5A, PKP2, RYR2, TNNI3, PRKAG2, PLN, DSG2, JUP, TNNT2, RBM20, ACTN2, DSC2
Specificity
6 %
Genes
34 %
Invitae Cardiomyopathy Comprehensive Panel.

By Invitae in United States.

TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, GLA, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC , (...)

View the complete list with 30 more genes
Specificity
2 %
Genes
34 %
Invitae Dilated Cardiomyopathy Panel.

By Invitae in United States.

TTR, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, BAG3, MYBPC3, TMEM43 , (...)

View the complete list with 21 more genes
Specificity
3 %
Genes
34 %
Invitae Left Ventricular Noncompaction Panel.

By Invitae in United States.

DSP, TAZ, LMNA, MYH7, MYBPC3, HCN4, SCN5A, LAMP2, RYR2, ACTC1, TNNI3, PLN, TPM1, TNNT2, VCL
Specificity
7 %
Genes
34 %
Invitae Cardiomyopathy and Skeletal Muscle Disease Panel.

By Invitae in United States.

TTR, AGL, GAA, EYA4, CPT2, GNE, TRIM32, DSP, CRYAB, RAF1, VCP, DPM3, PNPLA2, DPM1, SQSTM1, TAZ, SLC22A5, DOLK, DMD, GLA , (...)

View the complete list with 93 more genes
Specificity
1 %
Genes
34 %
Invitae Long QT Syndrome Panel.

By Invitae in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, CALM2, TRDN, KCNE2, CALM3
Specificity
8 %
Genes
34 %
Invitae Brugada Syndrome Panel.

By Invitae in United States.

KCNH2, HCN4, SCN5A, CACNA1C, ABCC9, CACNB2, GPD1L, PKP2
Specificity
13 %
Genes
34 %
Brugada syndrome: SCN5A gene sequence analysis.

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

SCN5A
Specificity
100 %
Genes
34 %
Dilated cardiomyopathy: SCN5A gene sequence analysis.

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

SCN5A
Specificity
100 %
Genes
34 %
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
34 %
BRUGADA SYNDROME.

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

KCND3, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1C, TRPM4, KCNJ8, SCN3B, KCNE3, CACNB2, GPD1L, RANGRF, KCNE5
Specificity
8 %
Genes
34 %
CARDIOMYOPATHY, DILATED (DCM.

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

TTR, PSEN1, EYA4, TAZ, DMD, LMNA, PSEN2, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, TCAP, SGCD, SCN5A, LAMP2, ACTC1, ANKRD1, TNNC1 , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
34 %
LONG QT SYNDROME.

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

CAV3, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, RYR2, CALM1, TRDN, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B, KCNA5 , (...)

View the complete list with 3 more genes
Specificity
5 %
Genes
34 %
Catecholaminergic Polymorphic Ventricular Tachycardia.

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

KCNJ2, SCN5A, ANK2, RYR2, CALM1, TRDN, CASQ2
Specificity
15 %
Genes
34 %
Dilated Cardiomyopathy: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

TTR, DSP, CRYAB, TAZ, DMD, FKTN, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, PDLIM3 , (...)

View the complete list with 19 more genes
Specificity
3 %
Genes
34 %
Brugada Syndrome: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

SCN1B, HCN4, SCN5A, CACNA1C, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
13 %
Genes
34 %
Arrhythmias: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

DSP, TMEM43, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, TRPM4, KCNJ8, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2 , (...)

View the complete list with 17 more genes
Specificity
9 %
Genes
100 %
Long and Short QT Syndrome: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, KCNE2, SNTA1, AKAP9, SCN4B
Specificity
9 %
Genes
34 %
Sudden Cardiac Arrest (SCA): Sequencing and Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, ANK2, RYR2, KCNE2, CASQ2
Specificity
10 %
Genes
34 %
Comprehensive Cardiovascular: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

TTR, GAA, COL3A1, DSP, CRYAB, RAF1, FBN1, TAZ, CBS, SLC22A5, COL5A1, COL5A2, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11 , (...)

View the complete list with 97 more genes
Specificity
3 %
Genes
100 %
Arrhythmias: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

DSP, TMEM43, KCNJ2, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, KCNJ8, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, KCNE2, KCNJ5 , (...)

View the complete list with 9 more genes
Specificity
4 %
Genes
34 %
Brugada Syndrome: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

SCN1B, HCN4, SCN5A, CACNA1C, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
13 %
Genes
34 %
Cardiomyopathy: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

TTR, GAA, DSP, CRYAB, RAF1, TAZ, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SOS1, RIT1, MAP2K2, FKTN, LMNA, CAV3 , (...)

View the complete list with 42 more genes
Specificity
2 %
Genes
34 %
Cardiomyopathy: Sequencing Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

TTR, GAA, DSP, CRYAB, RAF1, TAZ, SLC22A5, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SOS1, RIT1, MAP2K2, FKTN, LMNA , (...)

View the complete list with 45 more genes
Specificity
2 %
Genes
34 %
Comprehensive Cardiovascular: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

TTR, GAA, COL3A1, DSP, CRYAB, RAF1, FBN1, TAZ, CBS, COL5A1, COL5A2, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SOS1 , (...)

View the complete list with 86 more genes
Specificity
1 %
Genes
34 %
Dilated Cardiomyopathy: Deletion/Duplication Panel.

By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.

TTR, DSP, CRYAB, TAZ, DMD, FKTN, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, NEBL , (...)

View the complete list with 17 more genes
Specificity
3 %
Genes
34 %
Familial Cardiomyopathy Full Gene Sequencing Panel.

By Integrated Genetics Westborough Integrated Genetics in United States.

TTR, EYA4, DSP, DNAJC19, TAZ, ALMS1, GLA, FKTN, LMNA, CAV3, DES, MYH7, LDB3, MYBPC3, TMEM43, EMD, TCAP, SGCD, SCN5A, LAMP2 , (...)

View the complete list with 26 more genes
Specificity
3 %
Genes
34 %
Familial Arrhythmia Full Gene Sequencing Panel.

By Integrated Genetics Westborough Integrated Genetics in United States.

DSP, CAV3, TMEM43, KCNJ2, KCNH2, SCN1B, SCN5A, KCNE1, KCNQ1, CACNA1C, CACNB2, GPD1L, PKP2, ANK2, RYR2, KCNE2, SNTA1, CASQ2, AKAP9, SCN4B , (...)

View the complete list with 10 more genes
Specificity
7 %
Genes
67 %
Arrhythmia NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

DSP, CPT1A, SLC25A20, LMNA, CAV3, DES, TMEM43, KCNJ2, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, KCNJ8, SCN3B, KCNE3, CACNB2 , (...)

View the complete list with 18 more genes
Specificity
8 %
Genes
100 %
Pan-Cardio NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

TTR, GAA, EYA4, JAG1, DSP, CRYAB, RAF1, MRPL3, NDUFAF1, TAZ, COX15, FXN, SDHA, DOLK, DMD, GLA, PTPN11, FKTN, LMNA, PSEN2 , (...)

View the complete list with 81 more genes
Specificity
3 %
Genes
100 %
Long QT syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B
Specificity
8 %
Genes
34 %
Atrial Fibrillation NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

LMNA, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, KCNJ8, ABCC9, SCN2B, SCN3B, RYR2, KCNE2, KCNJ5, SCN4B, KCNA5, GATA4, GATA6 , (...)

View the complete list with 3 more genes
Specificity
14 %
Genes
100 %
Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MTHFR, UBE3A, PC, ARG1, BTD, ATPAF2, BCS1L, C12orf65, ADSL, PAX6, CPT2, PSAP, GNPTAB, GLB1, CC2D2A, PRODH, ATP6V0A2, GNE, HSD17B10, TMEM67 , (...)

View the complete list with 323 more genes
Specificity
1 %
Genes
34 %
Sudden Death Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

PSEN1, EYA4, DSP, SLC25A4, FBN1, TAZ, FKTN, LMNA, PSEN2, CAV3, TTN, DES, MYH7, LDB3, MYBPC3, TMEM43, TCAP, SGCD, KCNJ2, KCNH2 , (...)

View the complete list with 48 more genes
Specificity
5 %
Genes
100 %
Nuclear-Mito NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

HTT, UBE3A, MUTYH, TP53, MCCC1, MCCC2, AARS2, ACACA, ACAD9, ACADL, ACADM, ACADS, ACADVL, ACAT1, YARS2, FBP1, PC, GYS2, UQCRQ, UQCRB , (...)

View the complete list with 484 more genes
Specificity
1 %
Genes
34 %
Brugada Syndrome NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

SCN1B, HCN4, SCN5A, CACNA1C, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
13 %
Genes
34 %
Hypertrophic Cardiomyopathy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

TTR, DSP, CRYAB, RAF1, TAZ, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SOS1, MAP2K2, FKTN, LMNA, CAV3, TTN, DES , (...)

View the complete list with 43 more genes
Specificity
2 %
Genes
34 %
SCN5A.

By Fulgent Genetics Fulgent Genetics in United States.

SCN5A
Specificity
100 %
Genes
34 %
Early-Onset Epileptic Encephalopathy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

UBE3A, AUH, ADSL, ADGRV1, POLG, MECP2, LIAS, SLC25A12, GAMT, GATM, STXBP1, CTSD, SLC25A22, SLC9A6, ALDH7A1, TPP1, CLN3, WWOX, FARS2, SLC6A8 , (...)

View the complete list with 113 more genes
Specificity
1 %
Genes
34 %
Comprehensive Epilepsy NGS Panel.

By Fulgent Genetics Fulgent Genetics in United States.

MTHFR, UBE3A, PC, ARG1, BTD, ATPAF2, AUH, BCS1L, TWNK, C12orf65, ADSL, PAX6, AMACR, CPT2, PSAP, GNPTAB, GLB1, CC2D2A, PRODH, ATP6V0A2 , (...)

View the complete list with 427 more genes
Specificity
1 %
Genes
34 %
Long QT Syndrome (LQTS) Panel.

By Blueprint Genetics in Finland.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, CALM2, KCNE2, KCNJ5, AKAP9, NOS1AP, CALM3, TECRL
Specificity
7 %
Genes
34 %
Brugada Syndrome Panel.

By Blueprint Genetics in Finland.

CAV3, KCNH2, SCN1B, HCN4, SCN5A, CACNA1C, TRPM4, SCN3B, CACNB2
Specificity
12 %
Genes
34 %
Atrial Fibrillation Panel.

By Blueprint Genetics in Finland.

LMNA, LDB3, KCNJ2, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, SCN3B, CACNB2, RYR2, KCNE2, KCNJ5, KCNA5, TBX5, GATA6, NUP155, SCN10A
Specificity
6 %
Genes
34 %
Cardiomyopathy Panel.

By Blueprint Genetics in Finland.

HFE, TTR, AARS2, ACAD9, AGL, ACADVL, GAA, ELAC2, CPT2, GLB1, TRIM32, DSP, SLC25A4, FOXRED1, NDUFAF2, CRYAB, HADHA, RAF1, VCP, MTO1 , (...)

View the complete list with 135 more genes
Specificity
1 %
Genes
34 %
Left Ventricular Non-Compaction Cardiomyopathy (LVNC) Panel.

By Blueprint Genetics in Finland.

DSP, RAF1, DMD, LMNA, TTN, DES, MYH7, FLNC, BAG3, MYBPC3, EMD, TCAP, HCN4, SCN5A, LAMP2, ABCC9, PKP2, RYR2, MYH6, PLN , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
34 %
Arrhythmia Panel.

By Blueprint Genetics in Finland.

DSP, HADHA, LMNA, CAV3, TTN, DES, LDB3, BAG3, TMEM43, KCNJ2, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, TRPM4, ABCC9, SCN3B , (...)

View the complete list with 35 more genes
Specificity
2 %
Genes
34 %
Comprehensive Cardiology Panel.

By Blueprint Genetics in Finland.

HFE, TTR, AARS2, ACAD9, AGL, ACADVL, GAA, ELAC2, CPT2, GLB1, TRIM32, DSP, SLC25A4, FOXRED1, NDUFAF2, CRYAB, HADHA, RAF1, VCP, MTO1 , (...)

View the complete list with 165 more genes
Specificity
1 %
Genes
34 %
Dilated Cardiomyopathy (DCM) Panel.

By Blueprint Genetics in Finland.

TTR, GLB1, DSP, RAF1, PCCB, PCCA, TAZ, MLYCD, GBE1, ETFB, ETFA, ETFDH, ALMS1, DOLK, DMD, FKTN, LMNA, DYSF, TTN, DES , (...)

View the complete list with 50 more genes
Specificity
2 %
Genes
34 %
Long QT syndrome type III.

By Bioarray in Spain.

SCN5A
Specificity
100 %
Genes
34 %
Brugada syndrome type I.

By Bioarray in Spain.

SCN5A
Specificity
100 %
Genes
34 %
Cardiomyopathy, dilated type 1E.

By Bioarray in Spain.

SCN5A
Specificity
100 %
Genes
34 %
Long QT syndrome type III.

By Bioarray in Spain.

SCN5A
Specificity
100 %
Genes
34 %
CardioGene Set.

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

TTR, DSP, RAF1, TAZ, BRAF, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, RIT1, MAP2K2, LMNA, CAV3, TTN, DES, MYH7 , (...)

View the complete list with 60 more genes
Specificity
2 %
Genes
34 %
Arrhythmia Gene Set.

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

CAV3, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, KCNJ8, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, KCNE2 , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
34 %
Brugada Syndrome Gene Set.

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

KCND3, SCN1B, HCN4, SCN5A, CACNA1C, KCNJ8, SCN3B, KCNE3, CACNB2, GPD1L, PKP2
Specificity
10 %
Genes
34 %
Long QT Syndrome Gene Set.

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

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B
Specificity
8 %
Genes
34 %
Cardiomyopathy Gene Set.

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

TTR, DSP, RAF1, TAZ, BRAF, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, RIT1, MAP2K2, LMNA, TTN, DES, MYH7, LDB3 , (...)

View the complete list with 39 more genes
Specificity
2 %
Genes
34 %
Dilated Cardiomyopathy Gene Set.

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

TAZ, LMNA, TTN, DES, MYH7, LDB3, BAG3, FHL1, MYBPC3, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, ACTC1, ANKRD1, TNNC1, TNNI3, MYH6 , (...)

View the complete list with 12 more genes
Specificity
4 %
Genes
34 %
Brugada Syndrome Panel.

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

KCND3, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1C, TRPM4, KCNJ8, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
8 %
Genes
34 %
Long QT Syndrome NGS and Deletion/Duplication Panel.

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

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, RYR2, CALM1, TRDN, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B, CALM3
Specificity
6 %
Genes
34 %
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
34 %
Comprehensive Cardiomyopathy Panel.

By ApolloGen, Inc. in United States.

TTR, PSEN1, TAZ, GLA, LMNA, MT-TL1, MT-TK, PSEN2, CAV3, DES, MYH7, LDB3, MYBPC3, TCAP, SGCD, SCN5A, MT-TS1, MT-TS2, LAMP2, ABCC9 , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
34 %
Dilated Cardiomyopathy Panel.

By ApolloGen, Inc. in United States.

PSEN1, TAZ, LMNA, MT-TL1, MT-TK, PSEN2, DES, MYH7, LDB3, MYBPC3, TCAP, SGCD, SCN5A, MT-TS1, MT-TS2, ABCC9, ACTC1, LAMA4, TNNI3, MYH6 , (...)

View the complete list with 13 more genes
Specificity
4 %
Genes
34 %
iGene Cardiac Panel.

By ApolloGen, Inc. in United States.

COL3A1, DSP, GLA, LDLR, LMNA, TTN, MYH7, MYBPC3, KCNH2, SCN5A, KCNQ1, PKP2, RYR2, ACTC1, TNNI3, PRKAG2, DSG2, TPM1, TNNT2, MYL3 , (...)

View the complete list with 2 more genes
Specificity
5 %
Genes
34 %
Cardiomyopathy Exome Panel.

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

TTR, GAA, PSEN1, DSP, CRYAB, RAF1, TAZ, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, RIT1, MAP2K2 , (...)

View the complete list with 55 more genes
Specificity
2 %
Genes
34 %
Cardiac Arrhythmia Exome Panel.

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

DSP, GLA, LMNA, CAV3, TTN, DES, LDB3, TMEM43, EMD, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA1D, KCNE1, KCNQ1, CACNA1C, TRPM4 , (...)

View the complete list with 31 more genes
Specificity
6 %
Genes
100 %
Brugada Syndrome Panel by NGS.

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

SCN5A
Specificity
100 %
Genes
34 %
Long QT Syndrome Panel by NGS.

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

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, CALM2, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B
Specificity
7 %
Genes
34 %
Familial Dilated Cardiomyopathy Panel by NGS.

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

DSP, RAF1, TAZ, DMD, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, PKP2, ACTC1, ANKRD1 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
34 %
Left Ventricular Noncompaction Panel by NGS.

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

DSP, RAF1, TAZ, DMD, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, PKP2, ACTC1, ANKRD1 , (...)

View the complete list with 15 more genes
Specificity
3 %
Genes
34 %
Ventricular Fibrillation, Familial Panel by NGS.

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

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, CALM2, KCNE2, KCNJ5, SNTA1, AKAP9, SCN4B
Specificity
7 %
Genes
34 %
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
34 %
Arrhythmogenic Right Ventricular Cardiomyopathy Panel by NGS.

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

DSP, LMNA, TTN, DES, TMEM43, SCN5A, PKP2, RYR2, TGFB3, PLN, DSG2, JUP, DSC2
Specificity
8 %
Genes
34 %
Channelopathies.

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

KCNH2, SCN5A, RYR2, CASQ2, KCNQ1-AS1
Specificity
20 %
Genes
34 %
FAMILIAL DILATED CARDIOMYOPATHY.

By Laboratorio de Genetica Clinica SL in Spain.

EYA4, LMNA, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, TCAP, SCN5A, ACTC1, ANKRD1, TNNC1, TNNI3, MYH6, PLN, NEXN, DSG2, TPM1, TNNT2 , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
34 %
BRUGADA SYNDROME.

By Laboratorio de Genetica Clinica SL in Spain.

SCN1B, HCN4, SCN5A, CACNA1C, TRPM4, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
12 %
Genes
34 %
LONG QT SYNDROME, ROMANO-WARD SYNDROME.

By Laboratorio de Genetica Clinica SL in Spain.

KCNH2, SCN5A, KCNE1, KCNQ1, KCNE2
Specificity
20 %
Genes
34 %
BRUGADA SYNDROME/LONG-QT/SHORT-QT/VENTRICULAR TACHYCARDIA: NGS PANEL.

By Laboratorio de Genetica Clinica SL in Spain.

KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, TRPM4, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2 , (...)

View the complete list with 5 more genes
Specificity
4 %
Genes
34 %
FAMILIAL DILATED CARDIOMYOPATHY/HYPERTROPHIC/NONCOMPACTION: NGS PANEL.

By Laboratorio de Genetica Clinica SL in Spain.

PSEN1, EYA4, DSP, CRYAB, RAF1, MRPL3, TAZ, DMD, FKTN, LMNA, PSEN2, TTN, DES, MYH7, FLNC, LDB3, BAG3, MYBPC3, TCAP, SGCD , (...)

View the complete list with 33 more genes
Specificity
2 %
Genes
34 %
Brugada Syndrome Type 1 , Sequencing SCN5A Gene.

By Reference Laboratory Genetics in Spain.

SCN5A
Specificity
100 %
Genes
34 %
Long QT Syndrome Type 3 , Sequencing SCN5A Gene.

By Reference Laboratory Genetics in Spain.

SCN5A
Specificity
100 %
Genes
34 %
Dilated Cardiomyopathy, Sequencing SCN5A Gene.

By Reference Laboratory Genetics in Spain.

SCN5A
Specificity
100 %
Genes
34 %
Dilated Cardiomyopathy, Panel Massive Sequencing (NGS) 30 Genes.

By Reference Laboratory Genetics in Spain.

TTR, PSEN1, EYA4, TAZ, DMD, LMNA, PSEN2, TTN, DES, MYH7, LDB3, BAG3, MYBPC3, TCAP, SGCD, SCN5A, LAMP2, ACTC1, TNNC1, TNNI3 , (...)

View the complete list with 10 more genes
Specificity
4 %
Genes
34 %
Brugada Syndrome, Panel Massive Sequencing (NGS) 8 Genes.

By Reference Laboratory Genetics in Spain.

SCN1B, HCN4, SCN5A, CACNA1C, SCN3B, KCNE3, CACNB2, GPD1L
Specificity
13 %
Genes
34 %
Long QT Syndrome , Panel Massive Sequencing (NGS) 11 Genes.

By Reference Laboratory Genetics in Spain.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, ANK2, KCNE2, SNTA1, AKAP9, SCN4B
Specificity
10 %
Genes
34 %
Familial Atrial Fibrillation , Panel Massive Sequencing (NGS) 13 Genes.

By Reference Laboratory Genetics in Spain.

KCNJ2, SCN1B, SCN5A, KCNQ1, ABCC9, SCN2B, SCN3B, KCNE2, SCN4B, KCNA5, NUP155, NPPA, GJA5
Specificity
24 %
Genes
100 %
Ventricular Arrhythmia and Sudden Cardiac Death , Panel Massive Sequencing (NGS) 48 Genes.

By Reference Laboratory Genetics in Spain.

ACADM, DSP, LMNA, CAV3, TTN, DES, FLNC, TMEM43, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA1D, KCNE1, KCNQ1, CACNA1C, LAMP2, TRPM4 , (...)

View the complete list with 28 more genes
Specificity
3 %
Genes
34 %
Cardiology Genetic Panel (Full) , Panel Massive Sequencing (NGS) 96 Genes.

By Reference Laboratory Genetics in Spain.

TTR, RET, EYA4, PITX2, DSP, CRYAB, DNM1L, SLC25A3, TSFM, DNAJC19, PHOX2A, TAZ, DMD, DMPK, PTPN11, PHOX2B, FKTN, LMNA, CAV3, TTN , (...)

View the complete list with 75 more genes
Specificity
4 %
Genes
100 %
Cardiac Conduction System Related Disorders , Panel Massive Sequencing (NGS) 20 Genes.

By Reference Laboratory Genetics in Spain.

TTR, GAA, GLA, LMNA, DES, EMD, KCNJ2, SCN1B, HCN4, SCN5A, CACNA1D, LAMP2, TRPM4, ACTC1, NKX2-5, PRKAG2, TBX5, GJA5, SCN10A, TNNI3K
Specificity
10 %
Genes
67 %
Long QT syndrome 3.

By Labor Dr. Wisplinghoff in Germany.

SCN5A
Specificity
100 %
Genes
34 %
Phosphorus Dilated Cardiomyopathy Including Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

TTR, ACADVL, EYA4, CPT2, DSP, CRYAB, RAF1, TMEM70, DNAJC19, TAZ, SLC22A5, ALMS1, SDHA, DOLK, DMD, FKTN, LMNA, FKRP, CAV3, TTN , (...)

View the complete list with 28 more genes
Specificity
3 %
Genes
34 %
Phosphorus Pan Arrhythmia Panel.

By Phosphorus Diagnostics LLC in United States.

DSP, LMNA, CAV3, TTN, DES, LDB3, TMEM43, EMD, KCNJ2, KCNH2, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, ABCC9, KCNE3, CACNB2, GPD1L , (...)

View the complete list with 22 more genes
Specificity
3 %
Genes
34 %
Phosphorus Pan Cardiomyopathy Panel.

By Phosphorus Diagnostics LLC in United States.

TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, GLA, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC , (...)

View the complete list with 32 more genes
Specificity
2 %
Genes
34 %
Phosphorus Pan Cardiomyopathy Including Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

TTR, AGL, ACADVL, GAA, ELAC2, EYA4, CPT2, DSP, CRYAB, RAF1, MTO1, TMEM70, DNAJC19, TAZ, SLC22A5, ALMS1, SDHA, DOLK, DMD, GLA , (...)

View the complete list with 40 more genes
Specificity
2 %
Genes
34 %
Phosphorus Pan Cardiomyopathy Including Rasopathies Panel.

By Phosphorus Diagnostics LLC in United States.

TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1 , (...)

View the complete list with 49 more genes
Specificity
2 %
Genes
34 %
Phosphorus Pan Arrhythmia and Cardiomyopathy Panel.

By Phosphorus Diagnostics LLC in United States.

TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, GLA, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC , (...)

View the complete list with 50 more genes
Specificity
2 %
Genes
34 %
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Rasopathies Panel.

By Phosphorus Diagnostics LLC in United States.

TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1 , (...)

View the complete list with 67 more genes
Specificity
2 %
Genes
34 %
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

TTR, AGL, ACADVL, GAA, ELAC2, EYA4, CPT2, DSP, CRYAB, RAF1, MTO1, TMEM70, DNAJC19, TAZ, SLC22A5, ALMS1, SDHA, DOLK, BRAF, DMD , (...)

View the complete list with 75 more genes
Specificity
2 %
Genes
34 %
Phosphorus Pan Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

TTR, AGL, ACADVL, GAA, ELAC2, EYA4, CPT2, DSP, CRYAB, RAF1, MTO1, TMEM70, DNAJC19, TAZ, SLC22A5, ALMS1, SDHA, DOLK, BRAF, DMD , (...)

View the complete list with 57 more genes
Specificity
2 %
Genes
34 %
Phosphorus Pan Arrhythmia and Cardiomyopathy Including Recessive Pediatric Syndromes Panel.

By Phosphorus Diagnostics LLC in United States.

TTR, AGL, ACADVL, GAA, ELAC2, EYA4, CPT2, DSP, CRYAB, RAF1, MTO1, TMEM70, DNAJC19, TAZ, SLC22A5, ALMS1, SDHA, DOLK, DMD, GLA , (...)

View the complete list with 58 more genes
Specificity
2 %
Genes
34 %
Phosphorus Brugada Syndrome Panel.

By Phosphorus Diagnostics LLC in United States.

KCNH2, HCN4, SCN5A, CACNA1C, ABCC9, KCNE3, CACNB2, GPD1L, PKP2, SCN10A
Specificity
10 %
Genes
34 %
Phosphorus Long QT Syndrome Panel.

By Phosphorus Diagnostics LLC in United States.

CAV3, KCNJ2, KCNH2, SCN5A, KCNE1, KCNQ1, CACNA1C, ANK2, CALM1, CALM2, TRDN, KCNE2, SNTA1, SCN4B, CALM3
Specificity
7 %
Genes
34 %
Phosphorus Arrhythmogenic Cardiomyopathy Panel.

By Phosphorus Diagnostics LLC in United States.

DSP, LMNA, TTN, DES, LDB3, TMEM43, EMD, SCN5A, PKP2, RYR2, TGFB3, TNNI3, PRKAG2, PLN, DSG2, JUP, TNNT2, RBM20, ACTN2, DSC2
Specificity
5 %
Genes
34 %
Phosphorus Dilated Cardiomyopathy Panel.

By Phosphorus Diagnostics LLC in United States.

TTR, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, LDB3, BAG3, MYBPC3 , (...)

View the complete list with 22 more genes
Specificity
3 %
Genes
34 %
Phosphorus Left Ventricular Noncompaction Panel.

By Phosphorus Diagnostics LLC in United States.

DSP, TAZ, LMNA, MYH7, LDB3, MYBPC3, HCN4, SCN5A, LAMP2, RYR2, ACTC1, TNNI3, PLN, TPM1, TNNT2, ACTN2, VCL
Specificity
6 %
Genes
34 %
Tempus xO assay.

By Tempus Labs, Inc. in United States.

BRCA1, BRCA2, VHL, APC, EPCAM, MSH2, PMS2, MSH6, MLH1, MUTYH, PTEN, RECQL4, RUNX1, TP53, ABCB11, ABCB4, FKBP10, FOXL2, HNF1A, PPARG , (...)

View the complete list with 1693 more genes
Specificity
1 %
Genes
34 %
NPPA.

By Institute for Human Genetics University Clinic Freiburg in Germany.

NPPA
Specificity
100 %
Genes
34 %
Atrial fibrillation, familial 6 (sequence analysis of NPPA gene).

By CGC Genetics in Portugal.

NPPA
Specificity
100 %
Genes
34 %
Atrial Fibrillation Syndrome via NPPA Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

NPPA
Specificity
100 %
Genes
34 %
Atrial fibrillation type 6.

By Centogene AG - the Rare Disease Company in Germany.

NPPA
Specificity
100 %
Genes
34 %
NPPA.

By Fulgent Genetics Fulgent Genetics in United States.

NPPA
Specificity
100 %
Genes
34 %
Study of Molecular Markers Of Essential Hypertension and Associated Cardiovascular Events (37 genes - 57 genetic variants).

By HeartGenetics, Genetics and Biotechnology, SA in Portugal.

WNK1, HSD11B2, SLC12A3, SCNN1A, SCNN1B, CLCNKB, CLCNKA, AGTR2, NEDD4L, GNB3, ACE, NR3C2, NPPA, REN, NOS3, AGT, ECE1, ADRB2, AGTR1, STK39 , (...)

View the complete list with 6 more genes
Specificity
4 %
Genes
34 %
GJA5.

By Institute for Human Genetics University Clinic Freiburg in Germany.

GJA5
Specificity
100 %
Genes
34 %
Atrial fibrillation, familial 11 (sequence analysis of GJA5 gene).

By CGC Genetics in Portugal.

GJA5
Specificity
100 %
Genes
34 %
Atrial Fibrillation via GJA5 Gene Sequencing with CNV Detection.

By PreventionGenetics PreventionGenetics in United States.

GJA5
Specificity
100 %
Genes
34 %
Atrial fibrillation type 11.

By Centogene AG - the Rare Disease Company in Germany.

GJA5
Specificity
100 %
Genes
34 %
Congenital Heart Defects Panel.

By CeGaT GmbH in Germany.

ELN, FOXC1, PITX2, JAG1, CHD7, MYH7, FLNA, TBX1, SEMA3E, RBM10, NODAL, FOXH1, NOTCH1, ACTC1, NKX2-5, MYH6, TBX5, GJA1, SMAD2, ZIC3 , (...)

View the complete list with 24 more genes
Specificity
3 %
Genes
34 %
Congenital Heart Diseases Panel.

By Health in Code in Spain.

ELN, EYA4, PITX2, JAG1, RAF1, BRAF, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, MAP2K2, CBL, TTN, MYH7, MYBPC3, FLNA, TBX1 , (...)

View the complete list with 19 more genes
Specificity
3 %
Genes
34 %
Congenital heart diseases Panel.

By Health in Code in Spain.

ELN, EYA4, FOXC1, PITX2, JAG1, NPHP4, RAF1, BRAF, CHD7, CREBBP, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, MAP2K2, CBL, NF1 , (...)

View the complete list with 56 more genes
Specificity
2 %
Genes
34 %
GJA5.

By Fulgent Genetics Fulgent Genetics in United States.

GJA5
Specificity
100 %
Genes
34 %
Congenital Structural Heart Disease Panel.

By Blueprint Genetics in Finland.

ELN, PITX2, JAG1, BCOR, CHD7, DHCR7, HRAS, SOS2, CBL, NSD1, GPC3, ENG, NF1, FLNA, TBX1, ACTB, ACTG1, HOXA1, RBM10, NODAL , (...)

View the complete list with 42 more genes
Specificity
2 %
Genes
34 %

Alternate names

Atrial Standstill 1; Atrst1 Is also known as atrial cardiomyopathy with heart block, cardiomyopathy, familial, with conduction disturbance;atrial cardiomyopathy with heart block.



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