| Panel Name, Specifity and genes Tested/covered | 
| Distal Myopathy Advanced Sequencing Evaluation. 
 By Athena Diagnostics Inc in United States.
 
GNE, CRYAB, VCP, NEB, DNM2, CAV3, DYSF, TTN, KLHL9, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3
 
Specificity
6 %
 
Genes
100 %
 | 
| Myofibrillar Myopathy Advanced Sequencing Evaluation. 
 By Athena Diagnostics Inc in United States.
 
CRYAB, TTN, DES, FLNC, MYOT, LDB3, BAG3, FHL1, SELENON
 
Specificity
12 %
 
Genes
100 %
 | 
| Neuromuscular Disorders Panel. 
 By Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center in United States.
 
ATP7A, TWNK, GAA, GNE, TRIM32, POLG, SLC25A4, GARS, RRM2B, CRYAB, VCP, AGK, CAVIN1, DPM3, SUCLA2, PNPLA2, REEP1, POLG2, TK2, DPM1	, (...)
View the complete list with 124 more genes 
ATP7A, TWNK, GAA, GNE, TRIM32, POLG, SLC25A4, GARS, RRM2B, CRYAB, VCP, AGK, CAVIN1, DPM3, SUCLA2, PNPLA2, REEP1, POLG2, TK2, DPM1, TYMP, PHKA1, CHAT, SUCLG1, PYGM, PMM2, MGME1, DMD, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, FIG4, TRPV4, HSPB8, HSPB1, DNM2, LMNA, CLCN1, PABPN1, FKRP, CAV3, UBA1, DYSF, SCN4A, SGCE, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, ATP2A1, BSCL2, BAG3, FHL1, SELENON, CACNA1S, RYR1, SETX, DCTN1, KLHL40, TPM3, ACTA1, CCDC78, MEGF10, KBTBD13, CNTN1, CFL2, TPM2, MYH2, TNNT1, MTM1, BIN1, BICD2, DYNC1H1, VRK1, IGHMBP2, SYNE1, TMEM43, SYNE2, EMD, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, SMCHD1, COLQ, MUSK, CHRNA1, CHRND, CHRNB1, SIL1, LAMA2, B4GAT1, DPM2, POMGNT2, CHKB, COL6A2, RXYLT1, COL6A3, LARGE1, COL6A1, B3GALNT2, ITGA7, DNMT1, CHRNG, LAMP2, LAS1L, PLEKHG5, HINT1, GAN, FBXL4, AMPD1, COL12A1, GLE1, KLHL41, LIMS2, MYF6, TNPO3, TNNI2, MTMR14, HNRNPDL, SLC5A7, TOR1AIP1, POMK, STAC3, SPEG, LMOD3, GMPPB	
Specificity
1 %
 
Genes
100 %
 | 
| Comprehensive Neuromuscular Panel. 
 By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.
 
GAA, GNE, TRIM32, CRYAB, VCP, CAVIN1, CHAT, PYGM, PMM2, DMD, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN	, (...)
View the complete list with 59 more genes 
GAA, GNE, TRIM32, CRYAB, VCP, CAVIN1, CHAT, PYGM, PMM2, DMD, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, DNM2, LMNA, PABPN1, FKRP, CAV3, DYSF, SCN4A, SGCE, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, BSCL2, BAG3, FHL1, SELENON, RYR1, TPM3, ACTA1, CFL2, TPM2, MYH2, TNNT1, MTM1, BIN1, VRK1, IGHMBP2, SYNE1, SYNE2, EMD, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, COLQ, MUSK, CHRNA1, CHRND, CHRNB1, SIL1, LAMA2, COL6A2, COL6A3, LARGE1, COL6A1, ITGA7, CHRNG, RYR2, PLEKHG5, AMPD1, GLE1, TNNI2, MTMR14	
Specificity
2 %
 
Genes
100 %
 | 
| Limb-Girdle Muscular Dystrophy. 
 By Knight Diagnostic Laboratories - Molecular Diagnostic Center Oregon Health & Science University in United States.
 
GAA, GNE, TRIM32, VCP, DMD, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT	, (...)
View the complete list with 14 more genes 
GAA, GNE, TRIM32, VCP, DMD, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, SYNE1, SYNE2, EMD, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, COL6A2, COL6A3, COL6A1	
Specificity
3 %
 
Genes
100 %
 | 
| Neuromuscular Disorders Sequencing Panel. 
 By Genetic Services Laboratory University of Chicago in United States.
 
GAA, GNE, TRIM32, CRYAB, VCP, DPM3, DPM1, ALG2, CHAT, PYGM, GBE1, DPAGT1, DMD, HRAS, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB	, (...)
View the complete list with 91 more genes 
GAA, GNE, TRIM32, CRYAB, VCP, DPM3, DPM1, ALG2, CHAT, PYGM, GBE1, DPAGT1, DMD, HRAS, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, DNM2, LMNA, FKRP, CAV3, DYSF, SCN4A, LAMB2, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, BAG3, FHL1, SELENON, RYR1, KLHL40, TPM3, ACTA1, CCDC78, MEGF10, KBTBD13, CNTN1, CFL2, TPM2, MYH2, TNNT1, MTM1, BIN1, SYNE1, TMEM43, SYNE2, EMD, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, TCAP, SGCD, ISPD, COLQ, MUSK, GFPT1, AGRN, CHRNA1, CHRND, CHRNB1, SIL1, LAMA2, B4GAT1, DPM2, CHKB, COL6A2, RXYLT1, COL6A3, LARGE1, COL6A1, B3GALNT2, ITGA7, SNAP25, LAMP2, FKBP14, TNXB, CHST14, MYL2, COL12A1, KLHL41, LIMS2, MYF6, TNPO3, HNRNPDL, POMK, STAC3, SPEG, LMOD3, GMPPB, STIM1, ORAI1, COL13A1, HACD1, SYT2, PREPL, LRP4, ALG14	
Specificity
1 %
 
Genes
100 %
 | 
| Limb-Girdle Muscular Dystrophy Sequencing Panel. 
 By Genetic Services Laboratory University of Chicago in United States.
 
GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, TRAPPC11, DNAJB6, DAG1	, (...)
View the complete list with 11 more genes 
GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, LIMS2, TNPO3, HNRNPDL, POMK, GMPPB	
Specificity
4 %
 
Genes
100 %
 | 
| Limb-Girdle Muscular Dystrophy Deletion/Duplication Panel. 
 By Genetic Services Laboratory University of Chicago in United States.
 
GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, TRAPPC11, DNAJB6, DAG1	, (...)
View the complete list with 11 more genes 
GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, LIMS2, TNPO3, HNRNPDL, POMK, GMPPB	
Specificity
4 %
 
Genes
100 %
 | 
| FLNC. Complete sequencing. 
 By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.
 
FLNC
 
Specificity
100 %
 
Genes
100 %
 | 
| FLNC. Complete sequencing. 
 By Instituto de Medicina Genomica Instituto de Medicina Genomica in Spain.
 
FLNC
 
Specificity
100 %
 
Genes
100 %
 | 
| Filaminopathy (sequence analysis of FLNC gene). 
 By CGC Genetics in Portugal.
 
FLNC
 
Specificity
100 %
 
Genes
100 %
 | 
| Distal Hereditary Myopathy Sequencing Panel. 
 By PreventionGenetics PreventionGenetics in United States.
 
GNE, CRYAB, VCP, SQSTM1, CAV3, DYSF, TTN, KLHL9, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1, DNAJB6, TCAP
 
Specificity
5 %
 
Genes
100 %
 | 
| Myofibrillar Myopathy via the FLNC Gene. 
 By PreventionGenetics PreventionGenetics in United States.
 
FLNC
 
Specificity
100 %
 
Genes
100 %
 | 
| Comprehensive Neuromuscular Sequencing Panel. 
 By PreventionGenetics PreventionGenetics in United States.
 
AGL, GAA, GNE, TRIM32, CRYAB, VCP, CAVIN1, DPM3, PNPLA2, DPM1, ALG2, SQSTM1, ISCU, CHAT, PFKM, PYGM, GBE1, DPAGT1, DMD, CHRNE	, (...)
View the complete list with 104 more genes 
AGL, GAA, GNE, TRIM32, CRYAB, VCP, CAVIN1, DPM3, PNPLA2, DPM1, ALG2, SQSTM1, ISCU, CHAT, PFKM, PYGM, GBE1, DPAGT1, DMD, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, DNM2, LMNA, CLCN1, FKRP, CAV3, DYSF, SCN4A, TTN, KLHL9, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, ATP2A1, BAG3, FHL1, SELENON, CACNA1S, RYR1, KLHL40, TPM3, ACTA1, CCDC78, MEGF10, KBTBD13, CNTN1, CFL2, TPM2, MYH2, TNNT1, MTM1, BIN1, BICD2, SYNE1, TMEM43, EMD, TRAPPC11, DNAJB6, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, SMCHD1, COLQ, MUSK, GFPT1, AGRN, CHRNA1, CHRND, CHRNB1, SIL1, LAMA2, B4GAT1, DPM2, POMGNT2, CHKB, COL6A2, RXYLT1, COL6A3, LARGE1, COL6A1, B3GALNT2, ITGA7, SNAP25, CHRNG, COL12A1, GLE1, KLHL41, LIMS2, TNPO3, TNNI2, HNRNPDL, TOR1AIP1, POMK, STAC3, LMOD3, GMPPB, TNNT3, MYH3, ECEL1, STIM1, MICU1, COL13A1, SYT2, PREPL, ALG14, HNRNPA2B1, HNRNPA1, MYO18B	
Specificity
1 %
 
Genes
100 %
 | 
| Distal Myopathy NGS panel. 
 By Connective Tissue Gene Tests in United States.
 
GNE, CRYAB, VCP, SQSTM1, DNM2, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1, DNAJB6, TCAP
 
Specificity
5 %
 
Genes
100 %
 | 
| Distal Myopathy Comprehensive panel. 
 By Connective Tissue Gene Tests in United States.
 
GNE, CRYAB, VCP, SQSTM1, DNM2, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1, DNAJB6, TCAP
 
Specificity
5 %
 
Genes
100 %
 | 
| Distal Myopathy Deletion / Duplication panel. 
 By Connective Tissue Gene Tests in United States.
 
GNE, CRYAB, VCP, SQSTM1, DNM2, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1, DNAJB6, TCAP
 
Specificity
5 %
 
Genes
100 %
 | 
| Myofibrillar myopathy and related disorders NGS panel. 
 By Connective Tissue Gene Tests in United States.
 
CRYAB, DES, FLNC, MYOT, LDB3, BAG3, FHL1, ACTA1, DNAJB6, KY, PYROXD1
 
Specificity
10 %
 
Genes
100 %
 | 
| Limb girdle muscular dystrophy Comprehensive panel. 
 By Connective Tissue Gene Tests in United States.
 
GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, EMD, TRAPPC11	, (...)
View the complete list with 15 more genes 
GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, EMD, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, LARGE1, LIMS2, TNPO3, HNRNPDL, TOR1AIP1, POMK, GMPPB	
Specificity
3 %
 
Genes
100 %
 | 
| Myofibrillar myopathy and related disorders Comprehensive panel. 
 By Connective Tissue Gene Tests in United States.
 
CRYAB, DES, FLNC, MYOT, LDB3, BAG3, FHL1, ACTA1, DNAJB6, KY, PYROXD1
 
Specificity
10 %
 
Genes
100 %
 | 
| Limb girdle muscular dystrophy Deletion / Duplication panel. 
 By Connective Tissue Gene Tests in United States.
 
GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, EMD, TRAPPC11	, (...)
View the complete list with 15 more genes 
GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, EMD, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, LARGE1, LIMS2, TNPO3, HNRNPDL, TOR1AIP1, POMK, GMPPB	
Specificity
3 %
 
Genes
100 %
 | 
| Limb girdle muscular dystrophy NGS panel. 
 By Connective Tissue Gene Tests in United States.
 
GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, EMD, TRAPPC11	, (...)
View the complete list with 15 more genes 
GAA, TRIM32, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, EMD, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, LARGE1, LIMS2, TNPO3, HNRNPDL, TOR1AIP1, POMK, GMPPB	
Specificity
3 %
 
Genes
100 %
 | 
| Myofibrillar myopathy and related disorders Deletion / Duplication panel. 
 By Connective Tissue Gene Tests in United States.
 
CRYAB, DES, FLNC, MYOT, LDB3, BAG3, FHL1, ACTA1, DNAJB6, KY, PYROXD1
 
Specificity
10 %
 
Genes
100 %
 | 
| Histological Myofibrillar Myopathy. 
 By MGZ Medical Genetics Center in Germany.
 
GNE, CRYAB, VCP, LMNA, TTN, DES, FLNC, MYOT, LDB3, BAG3, FHL1, PLEC
 
Specificity
9 %
 
Genes
100 %
 | 
| FLNC. 
 By MGZ Medical Genetics Center in Germany.
 
FLNC
 
Specificity
100 %
 
Genes
100 %
 | 
| 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 
TTR, AARS2, ACAD9, ACADM, ACADS, AGL, ACADVL, GAA, ELN, CPT2, GNE, JAG1, DSP, CRYAB, RAF1, VCP, FBN1, MTO1, AGK, TMEM70, SLC25A3, PNPLA2, GFM1, SCO2, TAZ, COX15, CPT1A, GBE1, ETFB, ETFA, ETFDH, SLC22A5, SLC25A20, SDHA, BRAF, CHD7, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, FKTN, SGCA, SGCB, POMGNT1, SGCG, LMNA, FKRP, CAV3, NF1, TTN, DES, MYH7, FLNC, MYOT, LDB3, BAG3, FHL1, SELENON, MYBPC3, ACTA1, SYNE1, TMEM43, SYNE2, EMD, PLEC, POMT2, POMT1, TCAP, SGCD, KCNJ2, CHKB, LARGE1, KCNH2, SCN5A, KMT2D, ZEB2, TBX1, KCNE1, KCNQ1, CACNA1C, LZTR1, LAMP2, SPRED1, RASA2, RRAS, A2ML1, NODAL, FOXH1, NOTCH1, TGFBR1, TGFBR2, ABCC9, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, CASQ2, AKAP9, SCN4B, KDM6A, DNAH11, BMPR2, ACTC1, TGFB3, NKX2-5, ANKRD1, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, JUP, TPM1, TNNT2, MYOZ2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL, TBX5, GJA1, GDF1, GATA4, CITED2, CRELD1, GATA6, CFC1, NOTCH2, ZFPM2, ADAMTSL4, GATA5, TBX20, SMAD6, TAB2, MED13L, NR2F2, NKX2-6, TLL1	
Specificity
1 %
 
Genes
100 %
 | 
| Muscle Disease with Distal Myopathy. 
 By MGZ Medical Genetics Center in Germany.
 
AGL, GNE, CRYAB, VCP, PNPLA2, CHRNE, CAPN3, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1	, (...)
View the complete list with 8 more genes 
AGL, GNE, CRYAB, VCP, PNPLA2, CHRNE, CAPN3, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1, CCDC78, BICD2, TCAP, AGRN, CHRNA1, CHRND, CHRNB1, MYH14	
Specificity
4 %
 
Genes
100 %
 | 
| Muscle Weakness (Myopathy, Muscular Dystrophy). 
 By MGZ Medical Genetics Center in Germany.
 
TTR, ACAD9, ACADM, ACADS, AGL, ACADVL, TWNK, GAA, TUBB3, AMACR, CPT2, GNE, TRIM32, POLG, SLC25A4, GARS, RRM2B, MFN2, CRYAB, HADHA	, (...)
View the complete list with 159 more genes 
TTR, ACAD9, ACADM, ACADS, AGL, ACADVL, TWNK, GAA, TUBB3, AMACR, CPT2, GNE, TRIM32, POLG, SLC25A4, GARS, RRM2B, MFN2, CRYAB, HADHA, VCP, MTO1, AGK, TMEM70, CAVIN1, PGM1, SLC25A3, PNPLA2, POLG2, TK2, GFM1, HADHB, ALG2, SCO2, PUS1, TAZ, ABHD5, LPIN1, COX15, ISCU, CPT1A, CHAT, PFKM, PYGM, GBE1, ETFB, ETFA, ETFDH, SLC22A5, SLC25A20, SEPT9, KIF21A, SDHA, DPAGT1, DMD, PHOX2B, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, GDAP1, TRPV4, MPZ, NEFL, EGR2, DNM2, LMNA, CLCN1, FKRP, CAV3, UBA1, DYSF, SCN4A, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, HSPG2, BAG3, FHL1, SELENON, CACNA1S, RYR1, KLHL40, TPM3, ACTA1, CCDC78, MEGF10, KBTBD13, CNTN1, CFL2, TPM2, MYH2, TNNT1, MTM1, BIN1, BICD2, DYNC1H1, IGHMBP2, SYNE1, TMEM43, SYNE2, EMD, TRAPPC11, DNAJB6, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, SMCHD1, COLQ, MUSK, GFPT1, AGRN, CHRNA1, CHRND, CHRNB1, SIL1, LAMA2, B4GAT1, DPM2, POMGNT2, CHKB, COL6A2, RXYLT1, COL6A3, LARGE1, COL6A1, B3GALNT2, ITGA7, GOSR2, HNRNPU, SNAP25, CUL4B, MYH14, LAMP2, LAS1L, FKBP14, TNXB, HINT1, AARS, AMPD1, COL12A1, LIMS2, MYF6, TNPO3, MTMR14, TOR1AIP1, POMK, STAC3, GMPPB, PIEZO2, MYBPC1, FDX2, PGK1, HADH, STIM1, ORAI1, MICU1, PREPL, LRP4, ALG14, SLC52A3, GLRB, GLRA1, SLC6A5	
Specificity
1 %
 
Genes
100 %
 | 
| Muscle Weakness Manifesting in Adulthood / Limb-Girdle Muscular Dystrophy (AD and AR). 
 By MGZ Medical Genetics Center in Germany.
 
ACADM, AGL, ACADVL, GAA, CPT2, GNE, TRIM32, POLG, RRM2B, CRYAB, HADHA, VCP, PNPLA2, TK2, HADHB, PUS1, ABHD5, LPIN1, ISCU, PYGM	, (...)
View the complete list with 70 more genes 
ACADM, AGL, ACADVL, GAA, CPT2, GNE, TRIM32, POLG, RRM2B, CRYAB, HADHA, VCP, PNPLA2, TK2, HADHB, PUS1, ABHD5, LPIN1, ISCU, PYGM, GBE1, ETFB, ETFA, ETFDH, SLC22A5, DMD, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, TRPV4, DNM2, LMNA, CLCN1, FKRP, CAV3, DYSF, SCN4A, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1, SELENON, RYR1, ACTA1, MYH2, MTM1, BICD2, DYNC1H1, TMEM43, EMD, TRAPPC11, DNAJB6, PLEC, POMT2, POMT1, TCAP, SGCD, COLQ, GFPT1, CHRNA1, CHRND, CHRNB1, CHKB, COL6A2, COL6A3, LARGE1, COL6A1, HNRNPU, LAMP2, HINT1, LIMS2, TNPO3, TOR1AIP1, GMPPB, HADH, STIM1	
Specificity
2 %
 
Genes
100 %
 | 
| Myofibrillar Panel. 
 By FirmaLab in United States.
 
CRYAB, DES, FLNC, MYOT, LDB3, BAG3
 
Specificity
17 %
 
Genes
100 %
 | 
| 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 
TTR, EYA4, DSP, CRYAB, TAZ, DMD, GLA, FKTN, LMNA, CAV3, DES, MYH7, FLNC, MYOT, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, PKP2, RYR2, CASQ2, PDLIM3, ILK, NEBL, ACTC1, MYLK2, LAMA4, ANKRD1, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, JUP, MYPN, TPM1, TNNT2, GATAD1, JPH2, MYOZ2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, DTNA, VCL, TMPO, CALR3, TRIM63, MYOZ1	
Specificity
2 %
 
Genes
100 %
 | 
| Myofibrillar myopathy panel. 
 By Genome Diagnostics Laboratory University Medical Center Utrecht in Netherlands.
 
CRYAB, DES, FLNC, MYOT, LDB3, BAG3, FHL1
 
Specificity
15 %
 
Genes
100 %
 | 
| Myofibrillar myopathy panel. 
 By Centogene AG - the Rare Disease Company in Germany.
 
CRYAB, DES, FLNC, MYOT, LDB3, BAG3, FHL1, DNAJB6
 
Specificity
13 %
 
Genes
100 %
 | 
| Myopathy, distal type 4. 
 By Centogene AG - the Rare Disease Company in Germany.
 
FLNC
 
Specificity
100 %
 
Genes
100 %
 | 
| Filaminopathy. 
 By Centogene AG - the Rare Disease Company in Germany.
 
FLNC
 
Specificity
100 %
 
Genes
100 %
 | 
| 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 
F2, F5, FMR1, HTT, HFE, MTHFR, TTR, UBE3A, VHL, PTEN, AARS2, ABHD12, ACACA, ACAD9, ACADL, ACADM, ACADS, AGL, ACADVL, ACAT1, ALDOA, ALDOB, PC, UQCRQ, ARG1, UQCRB, TYROBP, ATP5F1E, ATP7A, ATP7B, ATPAF2, BCKDHA, BCKDHB, BCS1L, BEST1, TWNK, C12orf65, GAA, ADSL, MMACHC, FBLN5, PRKCG, APP, AMN, PAX6, TGFB1, PSEN1, TUBB3, MTR, RET, OPTN, GPR143, INPP5E, MTRR, AMACR, HSD17B4, CPT2, OPA1, KRT5, DTNBP1, WFS1, PSAP, GLB1, CC2D2A, ATP6V0A2, SRD5A3, GNE, HSD17B10, OCRL, ELOVL4, NDP, HPRT1, NHS, TMEM67, ARL6, NPHP3, NPHP1, MKKS, ADGRV1, CEP290, TTC8, TRIM32, SHH, PRPH2, AASS, DLD, POLG, NDUFS4, HSPD1, SLC25A19, SLC25A4, GARS, AFG3L2, FOXRED1, RRM2B, NDUFAF2, KIF1B, MFN2, CRYAB, PANK2, HADHA, RAF1, OPA3, FH, VCP, SMPD1, MECP2, CYP11B2, MTO1, COQ9, PDSS2, PDSS1, ACO2, NDUFA12, DDOST, NDUFB3, NDUFA9, AGK, ALDH18A1, HPS1, DNM1L, DGUOK, BOLA3, ACSF3, BLOC1S3, HPS6, HPS5, HPS4, HPS3, TMEM70, NFU1, PCK2, NDUFAF1, CCDC28B, TTC19, MTPAP, NDUFA10, NUBPL, SCP2, KARS, SPTLC2, ABAT, GFER, TLR3, TMEM126A, SLC25A12, DPM3, PGM1, LDHA, ENO3, GAMT, GATM, SPR, STXBP1, SUCLA2, COQ8A, RFT1, TUBA1A, GYS1, RARS2, COG1, COG8, DARS2, TUSC3, SLC25A3, PNPLA2, TSFM, HTRA2, REEP1, DNAJC19, POLG2, CTSD, ACADSB, TK2, SLC25A22, MPDU1, GFM1, FLVCR1, HADHB, DPM1, COG7, ALG9, ATIC, ALG1, AP3B1, ALG8, ALG2, GRN, COQ2, SPG7, ALG12, B4GALT1, PARK7, HMGCS2, PINK1, GCSH, GLDC, AMT, CISD2, SCO2, SLC35A1, GAD1, ALG6, TYMP, MPI, ETHE1, ALG3, PUS1, OTC, FRMD7, HCCS, PDHA1, GK, TIMM8A, TAZ, ABCB7, AIFM1, MAOA, PHKA1, ACSL4, SLC9A6, BCOR, ABCD1, MMADHC, LMBRD1, ABHD5, HEXA, GM2A, ALDH5A1, ALDH3A2, HEXB, LPIN1, PHYH, SLC35C1, ALDH7A1, ACOX1, PGAM2, PTS, QDPR, PAH, AGXT, MPV17, NDUFA2, COX15, SURF1, NDUFS8, NDUFS7, NDUFS3, NDUFAF6, CHAT, GUSB, GALNS, GNS, HGSNAT, NAGLU, SGSH, SDHAF1, NDUFAF3, NDUFA1, NDUFA11, NDUFAF4, NDUFS1, NDUFV1, NDUFV2, NDUFS6, NDUFS2, NDUFAF5, MCEE, MMAB, MMAA, MUT, DBT, SUCLG1, GALC, ALDH4A1, HK1, PFKM, PYGM, GBE1, ETFB, ETFA, ETFDH, GCDH, FXN, LRPPRC, FASTKD2, COX6B1, SLC3A1, ASS1, CYP27A1, SIX6, SLC22A5, SLC25A20, MGAT2, PMM2, PRKN, BBS7, BBS5, BBS12, MKS1, BBS9, BBS10, BBS4, BBS1, BBS2, APTX, ASL, TPP1, CLN3, ALMS1, HESX1, KIF21A, WWOX, SNCB, PNKD, SOD1, NEFH, GSN, TACO1, TMLHE, SLC6A8, MTFMT, SDHA, ABCD4, AGA, AHCY, ARSB, DOLK, DPAGT1, MOGS, HPD, TSHR, FGFR3, AR, ARSA, ASPA, ARX, ELP1, GBA, BRAF, CDKL5, CHD7, CREBBP, DHCR7, DMD, EIF2B1, FOXG1, GJC2, HRAS, IDS, IDUA, IKBKG, KRAS, MEF2C, NPC1, NPC2, NRAS, PCDH19, PLP1, PORCN, PTPN11, RAI1, SHOC2, SLC2A1, SMN1, SOS1, WDR62, FGFR2, HDAC8, TSC2, RAD21, CBL, SYNGAP1, SMC3, SMC1A, TSC1, NIPBL, NSD1, ATM, MRE11, NBN, PTCH1, PHOX2B, MET, GPC3, RAD50, CHRNE, CLN6, CLN8, DOK7, FKTN, NEB, PEX2, PROP1, PPT1, PEX7, SGCA, SGCB, SACS, TH, MLC1, PEX1, POMGNT1, SGCG, SLC12A6, SLC17A5, SUMF1, TTPA, ABCC8, CAPN3, CLN5, EIF2B5, PLA2G6, RAPSN, TMEM216, NDRG1, SBF2, PRX, FIG4, FGD4, SH3TC2, MTMR2, GDAP1, TRPV4, MPZ, PMP22, NEFL, HSPB8, LITAF, RAB7A, EGR2, HSPB1, YARS, DNM2, LMNA, GJB1, NTRK1, WNK1, SPTLC1, ATL1, ZFYVE26, EIF2B3, SMN2, EIF2B2, EIF2B4, SPG11, CSTB, SCN1A, PSEN2, MAPT, APOE, C9orf72, AHI1, NOTCH3, CLCN1, FKRP, CAV3, UBA1, CNBP, DYSF, SCN4A, ATXN3, CACNA1A, TOR1A, THAP1, GCH1, NF1, LRRK2, SGCE, SNCA, FGFR1, KCNJ11, CASR, INS, INF2, LAMB2, BSND, CLCNKB, KCNJ1, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, MATR3, SPAST, KIF5A, ATP2A1, L1CAM, NIPA1, SLC33A1, BSCL2, WASHC5, RTN2, BAG3, FHL1, SELENON, PNPLA6, KIF1A, CYP7B1, AP5Z1, FA2H, SPART, SPG21, ALS2, CACNA1S, RYR1, SIGMAR1, FUS, SETX, DCTN1, CHMP2B, TARDBP, ANG, VAPB, PFN1, UBQLN2, TPM3, ACTA1, CCDC78, KBTBD13, CNTN1, CFL2, TPM2, TNNT1, MTM1, BIN1, BICD2, DYNC1H1, HSPB3, VRK1, IGHMBP2, SYNE1, SYNE2, EMD, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, SMCHD1, KCNA1, CACNB4, SLC1A3, COLQ, MUSK, GFPT1, AGRN, CHRNA1, CHRND, CHRNB1, SYT14, ANO10, TDP1, SIL1, GRM1, VAMP1, EEF2, KCND3, KCNC3, ITPR1, PDYN, FGF14, TGM6, TTBK2, SPTBN2, LAMA2, POMGNT2, COL6A2, COL6A3, LARGE1, COL6A1, MCPH1, ASPM, ATP1A2, ATP1A3, CACNA1H, CHRNB2, CPA6, EFHC1, LGI1, GABRB3, GOSR2, NHLRC1, KCTD7, PRICKLE1, PRICKLE2, SCN9A, SLC19A3, ST3GAL5, SCN1B, SCN2A, SYNJ1, SLC35A2, SLC6A1, FOLR1, GABRD, GRIN2B, KCNT1, KCNQ2, KCNQ3, PNPO, SCN3A, CHRNA2, CHRNA4, CHD2, EPM2A, GABRA1, GABRG2, GRIN2A, MBD5, KCNMA1, SCARB2, SCN5A, ALG13, ASAH1, TBC1D24, DEPDC5, PRRT2, BRAT1, PIGO, BCKDK, COL4A1, ARFGEF2, CENPJ, DCX, EMX2, QARS, NDE1, PQBP1, RAB3GAP1, SIX3, RELN, TUBA8, FLNA, TSEN54, PAFAH1B1, ADGRG1, STIL, SRPX2, TUBB2B, KRIT1, DNAJC5, MFSD8, ATP13A2, CCM2, PDCD10, KMT2D, RBFOX1, MAGI2, SETD2, TBL1XR1, SLC13A5, NEXMIF, SZT2, WDR45, ST3GAL3, ROGDI, SCN8A, PIGA, NRXN1, GRIN1, DYRK1A, PIGN, PIGV, ANKRD11, PLCB1, SPTAN1, PNKP, SAMHD1, KCNJ10, TCF4, RNASEH2A, RNASEH2C, RNASEH2B, CNTNAP2, SERPINI1, OFD1, SMS, ATRX, IQSEC2, FGD1, PHF6, SYP, GRIA3, ARHGEF9, PAK3, KDM5C, SYN1, OPHN1, ATP6AP2, CASK, CUL4B, RAB39B, SETBP1, ZEB2, TREX1, VPS13B, GFAP, VPS13A, TBX1, LBR, ATP2A2, HTRA1, SHANK3, SHANK2, ACTB, ACTG1, CACNA1D, EDN3, ERCC2, NLRP3, DNMT1, EDNRB, SOX10, PRPS1, CHSY1, GJB3, MYH14, MYH9, PEX6, TFAP2A, DIAPH3, ADNP, MID1, MED12, LAMC3, KIRREL3, FOXP2, FOXP1, EHMT1, CACNA1C, AP1S2, CHD8, HOXA1, TMEM231, ARID1B, CTNNB1, NLGN4X, NLGN3, PEX14, PEX19, PEX13, PEX3, PEX16, PEX26, PEX10, PEX12, PEX5, KAT6B, CLCNKA, MVK, FOXP3, NEU1, CHRNG, PHF8, IGBP1, HUWE1, AFF2, MBTPS2, LAMP2, MAGT1, ZNF711, FANCB, DKC1, DLG3, EBP, TSPAN7, UBE2A, UPF3B, USP9X, ZDHHC15, GDI1, FTSJ1, RPS6KA3, SHROOM4, RBM10, RPL10, RAB40AL, ZDHHC9, BRWD3, CLIC2, TAF1, SLC16A2, SOX3, NAA10, NSDHL, ARHGEF6, ZNF81, IL1RAPL1, KLF8, ZCCHC12, MSX2, TWIST1, NSUN2, CLCN2, NEDD4L, MTOR, VANGL1, EXOSC3, TSEN34, TSEN2, TGIF1, ZIC2, CEP152, CDON, GLI2, CDK5RAP2, FLVCR2, PCNT, ATR, NAGA, HYAL1, TGFB2, TGFBR1, TGFBR2, SKI, ACTA2, ABCC6, NFIX, RNF135, GLI3, TP63, MAGEL2, KDM6A, MARS, COX6A1, PLEKHG5, TRIM2, PDK3, SBF1, GNB4, DHTKD1, DNAJB2, HINT1, TFG, LRSAM1, AARS, MED25, GAN, IFT140, BLOC1S6, SLC4A4, ACVRL1, DOCK8, CSF2RB, NKX2-1, PRKAG2, AMPD1, COL12A1, LIMS2, MYF6, TNPO3, MTMR14, HNRNPDL, SLC5A7, POMK, GMPPB, LZTFL1, IFT27, BBIP1, WDPCP, SDCCAG8, PIEZO2, CHMP1A, ERCC6, KMT2A, SMARCA4, SMARCB1, ARID1A, SMARCA2, ERLIN1, REEP2, MAG, PGAP1, ENTPD1, NT5C2, KIF1C, C19orf12, UCHL1, B4GALNT1, TUBB4A, GBA2, CYP2U1, DDHD2, TECPR2, DDHD1, ADAR, VPS37A, ERLIN2, RAB3GAP2, AP4S1, AP4B1, AP4E1, AP4M1, ZFYVE27, KIF11, CTDP1, PGK1, FGF10, SLC9A9, LHX4, ACE, CD320, ALX4, EP300, RNASET2, EFTUD2, ASXL1, CCT5, GNPAT, CTC1, NOD2, FTL, CP, COASY, DCAF17, BDNF, MASP1, VEGFA, B9D1, ZIC3, TTC21B, TMEM237, TMEM138, TCTN2, TCTN1, RPGRIP1L, KIF7, CEP41, CPLANE1, ARL13B, EOMES, PIK3CA, RAB18, IER3IP1, RBBP8, MYCN, VLDLR, MARS2, COX10, SCO1, COG4, ALG11, COG6, COG5, TMEM165, IL11RA, CSF1R, TREM2, PRNP, SORL1, TPK1, SLC20A2, FBXO7, EARS2, DRD2, SLC6A3, PCBD1, APOA1, B9D2, ABCA1, PTF1A, VPS35, GP1BA, A2M, FGA, MYO5A, VIPAS39, CD36, VAX1, FREM1, ALX1, B3GLCT, PIK3R2, AKT3, AKT1, SLC4A1, RBM8A, NHEJ1, XK, LPIN2, FADD, DST, COL7A1, RANBP2, PRKRA, NOTCH2, TCTN3, UNC93B1, TRAF3, TICAM1, NLRP12, OCLN, NTRK2, PIGL, PDE6D, CSPP1, WNT5A, HEPACAM, RIN2, ZNF423, DYNC2H1, GRIP1, ESCO2, DHH, ROR2, WNT7A, ICK, ARSE, MAMLD1, PREPL, ASNS, SNAP29, CCDC88C, MPDZ, LAMB1, MED17, ZNF335, CEP135, KNL1, CEP63, TTI2, TAF2, NDST1, CRADD, EPB41L1, CACNG2, ANK3, TECR, MED23, LRP2, LINS1, C12orf57, SOBP, CDH15, TRAPPC9, PRSS12, MAN1B1, GRIK2, CRBN, CC2D1A, CA8, CD96, ALX3, ORC1, RNU4ATAC, AMPD2, SEPSECS, ASXL3, TUBGCP6, TSHB, TG, TBCE, DNAJC6, ANO3, HPCA, BCAP31, GNAL, ADCY5, SLC30A10, ACY1, AAAS, ATP8A2, ATP2B3, CAMTA1, ATCAY, COL18A1, GRID2, NOL3, PIK3R5, ELOVL5, ERCC5, NAT8L, STUB1, ITM2B, LMNB1, MAPK10, RUBCN, ZNF592, COA5, WDR81, POLR3A, POLR3B, RNF170, CHCHD10, CWF19L1, SCN10A, AP1S1, DSC3, KCNE5, WNT10A, EIF4G1, IL1RN, ARHGAP31, CERS1, ASCL1, GDNF, RETREG1, NGF, ARHGEF10, HOXD10, FAM126A, COL4A2, GYG1, PEX11B, POGZ, TRPS1, IFRD1, NOP56, UMPS, GLRB, TFAP2B, CST3, GLRA1, IGF1, SLC6A5, DRD3, TRPM6, NOS3, HDAC4, CIZ1, LYZ, PDE8B, HPSE2, PLEKHG4, EXOC8, AIMP1, IRX5, WNT3, TUBA4A, MSX1, TMCO1, GIGYF2, SNCAIP, ERCC1, ZBTB16, FTO, CHRM3, EXOSC8, TRPM7, FBXO38, YWHAE, CACNA1B, ALAD, KANK1, UPB1, NECTIN1, PRRX1, NOG, ATP2B4, ZFR, WDR48, USP8, ARSI, STRADA, RBFOX3, NDUFA4, ERBB4, WAC, HERC2, KCNK9, ADK, FLRT1, NXF5, ELK1, NRG1, VDAC1, DNAH9, FZD9, CD59, JRK, ACKR1, CD207, CR1, CNTNAP4, CDK11A, RABGGTA, TNFSF4, FRG1, TAS2R38, CISH, SNX3, ICAM1, YAP1, ADAM10, ZBTB18, EIF4E, SNIP1, AANAT, KCNK18, XBP1, NOS2, TIRAP, TLR5, PRKCH, ALOX5AP, TNF, FCGR2B	
Specificity
1 %
 
Genes
100 %
 | 
| Congenital and Distal Myopathies Panel. 
 By CeGaT GmbH in Germany.
 
YARS2, TWNK, OPA1, GNE, TRIM32, POLG, RRM2B, CRYAB, VCP, SUCLA2, POLG2, TK2, PUS1, ISCU, NEB, DNM2, PABPN1, CAV3, DYSF, TTN	, (...)
View the complete list with 53 more genes 
YARS2, TWNK, OPA1, GNE, TRIM32, POLG, RRM2B, CRYAB, VCP, SUCLA2, POLG2, TK2, PUS1, ISCU, NEB, DNM2, PABPN1, CAV3, DYSF, TTN, KLHL9, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1, SELENON, RYR1, KLHL40, TPM3, ACTA1, CCDC78, MEGF10, KBTBD13, CNTN1, CFL2, TPM2, MYH2, TNNT1, MTM1, BIN1, PLEC, SIL1, COL6A2, COL6A3, COL6A1, MYH14, LAMP2, FKBP14, ACVR1, DNA2, COL12A1, KLHL41, MYF6, MTMR14, STAC3, SPEG, LMOD3, CASQ1, STIM1, ORAI1, MICU1, HACD1, CHCHD10, VMA21, MSTN, HNRNPA2B1, HNRNPA1	
Specificity
2 %
 
Genes
100 %
 | 
| Limb-Girdle Muscular Dystrophies Panel. 
 By CeGaT GmbH in Germany.
 
GAA, GNE, TRIM32, DPM3, DMD, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT	, (...)
View the complete list with 14 more genes 
GAA, GNE, TRIM32, DPM3, DMD, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, LAMA2, TNPO3, HNRNPDL, POMK, GMPPB	
Specificity
3 %
 
Genes
100 %
 | 
| Congenital Myopathy and Distal Myopathy NGS panel. 
 By Asper Biogene Asper Biogene LLC in Estonia.
 
GNE, CRYAB, VCP, SQSTM1, NEB, DNM2, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1, SELENON	, (...)
View the complete list with 21 more genes 
GNE, CRYAB, VCP, SQSTM1, NEB, DNM2, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1, SELENON, RYR1, KLHL40, TPM3, ACTA1, CCDC78, MEGF10, CNTN1, CFL2, TPM2, TNNT1, MTM1, DNAJB6, COL6A3, COL6A1, COL12A1, KLHL41, MYF6, MTMR14, STAC3, LMOD3, MICU1	
Specificity
3 %
 
Genes
100 %
 | 
| Left Ventricular Non-Compactation Panel. 
 By Health in Code in Spain.
 
DSP, DNAJC19, TAZ, MLYCD, DMD, PTPN11, LMNA, TTN, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, KCNH2, HCN4, KCNQ1, NOTCH1, RYR2, CASQ2	, (...)
View the complete list with 16 more genes 
DSP, DNAJC19, TAZ, MLYCD, DMD, PTPN11, LMNA, TTN, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, KCNH2, HCN4, KCNQ1, NOTCH1, RYR2, CASQ2, ACTC1, PRDM16, NKX2-5, ANKRD1, TNNC1, TNNI3, MYH6, PLN, TPM1, TNNT2, ACTN2, CSRP3, MYL2, MYL3, DTNA, MIB1	
Specificity
3 %
 
Genes
100 %
 | 
| Restrictive Cardiomyopathy Panel. 
 By Health in Code in Spain.
 
HFE, TTR, GLA, LMNA, TTN, DES, MYH7, FLNC, BAG3, FHL1, MYBPC3, ACTC1, TNNC1, TNNI3, MYPN, TPM1, TNNT2, ACTN2, MYL2, MYL3
 
Specificity
5 %
 
Genes
100 %
 | 
| 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 
HFE, TTR, AARS2, ACAD9, ACADM, AGL, ACADVL, ATPAF2, GAA, COL1A1, COL1A2, COL3A1, PSEN1, ELN, EYA4, GNPTAB, GLB1, PITX2, JAG1, DSP, DLD, SLC25A4, CRYAB, RAF1, FBN1, MTO1, MRPL3, LIAS, AGK, TMEM70, FAH, MRPS22, TSFM, DNAJC19, GFM1, COQ2, PDHA1, TAZ, PHKA1, COX15, SURF1, GUSB, MLYCD, CBS, COX6B1, SLC22A5, PMM2, ALMS1, COL5A1, COL5A2, DOLK, BRAF, DMD, GLA, HRAS, KRAS, LDLR, MAP2K1, NRAS, PLOD1, PTPN11, SHOC2, SOS1, MAP2K2, CBL, SMAD4, ENG, FKTN, SGCA, SGCB, CAPN3, LMNA, PSEN2, NOTCH3, FKRP, CAV3, TTN, DES, MYH7, FLNC, MYOT, LDB3, BSCL2, BAG3, FHL1, MYBPC3, ACTA1, TMEM43, EMD, TCAP, SGCD, KCNJ2, KCND3, LAMA2, KCNH2, SCN1B, HCN4, SCN5A, FLNA, CACNA2D1, TBX1, CACNA1D, KCNE1, KCNQ1, CACNA1C, LAMP2, SPRED1, TGFB2, NOTCH1, SMAD3, TGFBR1, TGFBR2, SKI, MYLK, FBN2, ACTA2, SLC2A10, MYH11, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, CASQ2, AKAP9, SCN4B, ACVRL1, BMPR1B, GDF2, KCNK3, CAV1, SMAD9, KCNA5, BMPR2, PDLIM3, NEBL, ACTC1, MYLK2, TGFB3, LAMA4, PRDM16, NKX2-5, ANKRD1, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, JUP, MYPN, RANGRF, TPM1, TNNT2, GATAD1, JPH2, MYOZ2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, DTNA, VCL, PRKG1, TBX5, GJA1, CTF1, FHL2, TXNRD2, TMPO, GATA4, CRELD1, CETP, PCSK9, APOB, APOA5, GATA6, NPPA, GJA5, AGPAT2, ANK3, OBSL1, SCN10A, CTNNA3, KCNE5, ADAMTSL4, APOC3, CAVIN4, TBX20, MIB1, CALR3, LRP6, KLF10, TRIM63, SMAD1, FOXD4, FHOD3	
Specificity
1 %
 
Genes
100 %
 | 
| Hypertrophic Cardiomyopathy Short Panel. 
 By Health in Code in Spain.
 
TTR, GLA, PTPN11, DES, MYH7, FLNC, MYBPC3, ACTA1, LAMP2, TNNC1, TNNI3, PRKAG2, TPM1, TNNT2, MYL2, MYL3
 
Specificity
7 %
 
Genes
100 %
 | 
| 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 
HFE, TTR, GAA, PSEN1, EYA4, GLB1, DSP, CRYAB, RAF1, DNAJC19, TAZ, SLC22A5, ALMS1, DOLK, BRAF, DMD, GLA, PTPN11, FKTN, SGCA, SGCB, LMNA, PSEN2, FKRP, CAV3, TTN, DES, MYH7, FLNC, MYOT, LDB3, BAG3, MYBPC3, ACTA1, TMEM43, EMD, TCAP, SGCD, KCNJ2, LAMA2, SCN5A, LAMP2, KCNJ8, ABCC9, PKP2, RYR2, PDLIM3, NEBL, ACTC1, LAMA4, PRDM16, NKX2-5, ANKRD1, TNNC1, TNNI3, MYH6, PLN, NEXN, DSG2, JUP, MYPN, TPM1, TNNT2, GATAD1, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL, CTF1, FHL2, TXNRD2, TMPO, GATA4, GATA6, CAVIN4, TBX20, FOXD4, FHOD3	
Specificity
2 %
 
Genes
100 %
 | 
| Skeletal Myopathy Panel. 
 By Health in Code in Spain.
 
AGL, GAA, DLD, SLC25A4, CRYAB, AGK, COQ2, TAZ, PHKA1, SURF1, SLC22A5, PMM2, DOLK, DMD, HRAS, FKTN, SGCA, SGCB, CAPN3, LMNA	, (...)
View the complete list with 26 more genes 
AGL, GAA, DLD, SLC25A4, CRYAB, AGK, COQ2, TAZ, PHKA1, SURF1, SLC22A5, PMM2, DOLK, DMD, HRAS, FKTN, SGCA, SGCB, CAPN3, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, MYOT, LDB3, BSCL2, BAG3, FHL1, ACTA1, TMEM43, EMD, TCAP, SGCD, KCNJ2, LAMA2, CACNA1C, LAMP2, KCNE3, TNNI3, PRKAG2, MYL2, MYL3, CAVIN4	
Specificity
3 %
 
Genes
100 %
 | 
| 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 
HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATPAF2, GAA, GNPTAB, GLB1, PITX2, DSP, DLD, SLC25A4, CRYAB, RAF1, MTO1, MRPL3, LIAS, AGK, TMEM70, FAH, MRPS22, TSFM, GFM1, COQ2, PDHA1, TAZ, PHKA1, COX15, SURF1, GUSB, MLYCD, COX6B1, SLC22A5, PMM2, BRAF, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, MAP2K2, LMNA, CAV3, TTN, DES, MYH7, FLNC, LDB3, BSCL2, BAG3, FHL1, MYBPC3, ACTA1, TMEM43, EMD, TCAP, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1D, KCNE1, KCNQ1, CACNA1C, LAMP2, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, CASQ2, AKAP9, SCN4B, KCNK3, KCNA5, PDLIM3, ACTC1, MYLK2, TGFB3, NKX2-5, ANKRD1, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, JUP, MYPN, RANGRF, TPM1, TNNT2, JPH2, MYOZ2, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL, TBX5, GJA1, CTF1, FHL2, GATA4, GATA6, NPPA, GJA5, AGPAT2, ANK3, OBSL1, SCN10A, CTNNA3, KCNE5, CAVIN4, CALR3, KLF10, TRIM63, FHOD3	
Specificity
1 %
 
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 
ACADM, DSP, LMNA, CAV3, DES, FLNC, TMEM43, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1D, KCNE1, KCNQ1, CACNA1C, LAMP2, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, CASQ2, AKAP9, SCN4B, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, RANGRF, TNNT2, DSC2, ANK3, SCN10A, CTNNA3, KCNE5	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATPAF2, GAA, PSEN1, ELN, EYA4, GNPTAB, GLB1, PITX2, JAG1, DSP, DLD, SLC25A4, CRYAB, RAF1, MTO1, MRPL3, LIAS, AGK, TMEM70, FAH, MRPS22, TSFM, DNAJC19, GFM1, COQ2, PDHA1, TAZ, PHKA1, COX15, SURF1, GUSB, MLYCD, COX6B1, SLC22A5, PMM2, ALMS1, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, MAP2K2, CBL, FKTN, SGCA, SGCB, LMNA, PSEN2, FKRP, CAV3, TTN, DES, MYH7, FLNC, MYOT, LDB3, BSCL2, BAG3, FHL1, MYBPC3, ACTA1, TMEM43, EMD, TCAP, SGCD, KCNJ2, LAMA2, KCNH2, HCN4, SCN5A, FLNA, TBX1, KCNQ1, LAMP2, SPRED1, NOTCH1, SMAD3, ACTA2, MYH11, KCNJ8, ABCC9, PKP2, ANK2, RYR2, CASQ2, PDLIM3, NEBL, ACTC1, MYLK2, TGFB3, LAMA4, PRDM16, NKX2-5, ANKRD1, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, JUP, MYPN, TPM1, TNNT2, GATAD1, JPH2, MYOZ2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, DTNA, VCL, TBX5, GJA1, CTF1, FHL2, TXNRD2, TMPO, GATA4, CRELD1, GATA6, GJA5, AGPAT2, OBSL1, CTNNA3, CAVIN4, TBX20, MIB1, CALR3, KLF10, TRIM63, FOXD4, FHOD3	
Specificity
1 %
 
Genes
100 %
 | 
| 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
100 %
 | 
| Hypertrophic Cardiomyopathy Extended Panel. 
 By Health in Code in Spain.
 
TTR, AARS2, ACAD9, AGL, ACADVL, ATPAF2, GAA, GNPTAB, GLB1, DLD, SLC25A4, CRYAB, RAF1, MTO1, MRPL3, LIAS, AGK, TMEM70, FAH, MRPS22	, (...)
View the complete list with 70 more genes 
TTR, AARS2, ACAD9, AGL, ACADVL, ATPAF2, GAA, GNPTAB, GLB1, DLD, SLC25A4, CRYAB, RAF1, MTO1, MRPL3, LIAS, AGK, TMEM70, FAH, MRPS22, TSFM, GFM1, COQ2, PDHA1, TAZ, PHKA1, COX15, SURF1, GUSB, MLYCD, COX6B1, SLC22A5, PMM2, BRAF, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, MAP2K2, LMNA, CAV3, TTN, DES, MYH7, FLNC, LDB3, BSCL2, BAG3, FHL1, MYBPC3, ACTA1, TCAP, LAMP2, KCNJ8, ANK2, RYR2, CASQ2, PDLIM3, ACTC1, MYLK2, ANKRD1, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, MYPN, TPM1, TNNT2, JPH2, MYOZ2, ACTN2, CSRP3, MYL2, MYL3, VCL, CTF1, FHL2, AGPAT2, OBSL1, CAVIN4, CALR3, KLF10, TRIM63, FHOD3	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
DSP, LMNA, TTN, DES, FLNC, LDB3, TMEM43, SCN5A, CTNNB1, PKP2, RYR2, CASQ2, TGFB3, PLN, DSG2, JUP, DSC2, CTNNA3, PKP4, PERP, PPP1R13L	
Specificity
5 %
 
Genes
100 %
 | 
| 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 
HFE, TTR, GAA, DSP, CAVIN1, GLA, LMNA, CAV3, DES, MYH7, FLNC, LDB3, SYNE1, TMEM43, SYNE2, EMD, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1D, KCNE1, KCNQ1, CACNA1C, LAMP2, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, CASQ2, AKAP9, SCN4B, KCNA5, ACTC1, NKX2-5, TNNC1, TNNI3, MYH6, PRKAG2, PLN, DSG2, JUP, RANGRF, TNNT2, DSC2, NOS1AP, TBX5, FHL2, NPPA, GJA5, ANK3, FGF12, SCN10A, KCNE5, CAVIN4, CALM3, TNNI3K, KCND2, KCNK17, IRX3	
Specificity
2 %
 
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 
HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATP5F1E, ATP7A, ATPAF2, B4GALT7, GAA, HNF1A, NEUROD1, PPARG, COL1A1, COL1A2, COL3A1, ELAC2, PSEN1, HNF1B, ELN, EYA4, CPT2, WFS1, GNPTAB, GLB1, FOXC1, PITX2, JAG1, NPHP4, PCDH15, DSP, DLD, SLC25A4, GCK, FOXRED1, CRYAB, RAF1, OPA3, FBN1, MTO1, MRPL3, LIAS, GPD1, AGK, DNM1L, TMEM70, FAH, IDH2, CAVIN1, SLC39A13, MRPS22, SLC25A3, PNPLA2, TSFM, DNAJC19, GFM1, MEF2A, COQ2, SCO2, PDHA1, TAZ, PHKA1, COX15, SURF1, GUSB, MLYCD, CBS, PYGM, FXN, COX6B1, SLC22A5, PMM2, ALMS1, ZFHX3, COL5A1, COL5A2, SDHA, DOLK, BRAF, CHD7, CREBBP, DMD, FOXF1, GLA, HRAS, KRAS, LDLR, LEP, LIPA, MAP2K1, NRAS, PLOD1, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, BMPR1A, SMAD4, ENG, ADAMTS2, FKTN, MTTP, SGCA, SGCB, CAPN3, LMNA, PSEN2, APOE, NOTCH3, FKRP, CAV3, NF1, CEL, KCNJ11, INS, PDX1, HNF4A, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, BSCL2, BAG3, FHL1, RYR1, MYBPC3, ACTA1, SYNE1, TMEM43, SYNE2, EMD, TCAP, SGCD, KCNJ2, KCND3, LAMA2, KCNH2, SCN1B, HCN4, SCN5A, FLNA, KMT2D, CACNA2D1, KANSL1, TBX1, CACNA1D, KCNE1, KCNQ1, MED12, FOXP1, EHMT1, CACNA1C, CTNNB1, LZTR1, RASA1, FOXP3, LAMP2, UPF3B, ZDHHC9, SPRED1, RASA2, RRAS, A2ML1, ABCB1, NODAL, FOXH1, TGFB2, NOTCH1, SMAD3, TGFBR1, TGFBR2, SKI, MYLK, FBN2, ACTA2, SLC2A10, MYH11, FKBP14, CHST14, ACVR1, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, CASQ2, AKAP9, SCN4B, ACVRL1, BMPR1B, GDF2, KCNK3, CAV1, SMAD9, EFEMP2, KCNA5, BMPR2, PDLIM3, ILK, NEBL, ACTC1, MYLK2, TGFB3, LAMA4, PRDM16, NKX2-5, ANKRD1, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, JUP, MYPN, RANGRF, TPM1, TNNT2, GATAD1, JPH2, MYOZ2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, DTNA, AMPD1, TOR1AIP1, SPEG, VCL, ZMPSTE24, PRKG1, MFAP5, NOS1AP, SALL4, TBX5, EP300, GJA1, FHL2, B3GAT3, ABCG5, ABCG8, CYP2D6, OBSCN, TXNRD2, TMPO, ZIC3, GDF1, GATA4, EVC, IER3IP1, NPC1L1, CITED2, LEFTY2, CRELD1, ACVR2B, CETP, SCARB1, APOA1, PCSK9, LDLRAP1, APOB, APOA5, LPL, LMF1, APOC2, GPIHBP1, ANGPTL3, ABCG1, LCAT, ABCA1, SLC2A2, AKT2, RFX6, PAX4, KLF11, BLK, GLIS3, NEUROG3, PTF1A, GATA6, EIF2AK3, PDGFRA, INSR, CFC1, XK, TDGF1, COL7A1, NPPA, GJA5, NOTCH2, TBC1D4, CIDEC, PLIN1, AGPAT2, ZFPM2, ANK3, OBSL1, FGF12, COA5, SCN10A, CTNNA3, KCNE5, ADAMTSL4, GATA5, APOC3, LIPC, PLTP, CHRM2, CAVIN4, SLCO1B1, EIF2AK4, TBX20, MIB1, CALR3, ASPH, CALM3, MYLIP, SAR1B, TFAP2B, SMAD6, TAB2, TNNI3K, CYP3A4, INSIG2, LRP6, PKP4, KLF10, TRIM63, COA6, MED13L, KCND2, MRPL44, NKX2-6, CYP3A5, MCTP2, IRX4, SMAD1, FOXD4, FHOD3, PERP, PPP1R13L, KCNK17, IRX3, SLC22A8, LPA, MYOM1, PPARA, NNT, SLC25A40, HAND2, GREM2, ISL1, TOPBP1, TRIB1, BMP10, CH25H	
Specificity
1 %
 
Genes
100 %
 | 
| Non-compaction cardiomyopathy. 
 By Health in Code in Spain.
 
DSP, DNAJC19, TAZ, MLYCD, DMD, PTPN11, LMNA, TTN, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, KCNH2, HCN4, KCNQ1, NOTCH1, RYR2, CASQ2	, (...)
View the complete list with 17 more genes 
DSP, DNAJC19, TAZ, MLYCD, DMD, PTPN11, LMNA, TTN, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, KCNH2, HCN4, KCNQ1, NOTCH1, RYR2, CASQ2, ACTC1, PRDM16, NKX2-5, ANKRD1, TNNC1, TNNI3, MYH6, PLN, TPM1, TNNT2, ACTN2, CSRP3, MYL2, MYL3, DTNA, MIB1, NNT	
Specificity
3 %
 
Genes
100 %
 | 
| Skeletal myopathy Panel. 
 By Health in Code in Spain.
 
AGL, GAA, DLD, SLC25A4, CRYAB, AGK, CAVIN1, SLC25A3, COQ2, SCO2, TAZ, PHKA1, SURF1, FXN, SLC22A5, PMM2, SDHA, DOLK, DMD, HRAS	, (...)
View the complete list with 37 more genes 
AGL, GAA, DLD, SLC25A4, CRYAB, AGK, CAVIN1, SLC25A3, COQ2, SCO2, TAZ, PHKA1, SURF1, FXN, SLC22A5, PMM2, SDHA, DOLK, DMD, HRAS, FKTN, SGCA, SGCB, CAPN3, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, BSCL2, BAG3, FHL1, ACTA1, SYNE1, TMEM43, SYNE2, EMD, TCAP, SGCD, KCNJ2, LAMA2, CACNA1C, LAMP2, KCNE3, TNNI3, PRKAG2, MYL2, MYL3, TOR1AIP1, SPEG, XK, CAVIN4	
Specificity
2 %
 
Genes
100 %
 | 
| Hypertrophic cardiomyopathy panel. 
 By Health in Code in Spain.
 
TTR, GLA, PTPN11, DES, MYH7, FLNC, MYBPC3, LAMP2, ACTC1, TNNC1, TNNI3, PRKAG2, PLN, TPM1, TNNT2, MYL2, MYL3
 
Specificity
6 %
 
Genes
100 %
 | 
| Dilated Cardiomyopathy Panel. 
 By Health in Code in Spain.
 
EYA4, DSP, CRYAB, DNAJC19, TAZ, ALMS1, DOLK, DMD, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, ANO5, BAG3, MYBPC3, ACTA1	, (...)
View the complete list with 19 more genes 
EYA4, DSP, CRYAB, DNAJC19, TAZ, ALMS1, DOLK, DMD, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, ANO5, BAG3, MYBPC3, ACTA1, EMD, ABCC9, PKP2, ACTC1, ANKRD1, TNNC1, TNNI3, PLN, DSG2, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, FHL2, COL7A1, CHRM2, FHOD3	
Specificity
3 %
 
Genes
100 %
 | 
| 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 
HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATP5F1E, ATPAF2, GAA, ELAC2, PSEN1, EYA4, GNPTAB, GLB1, PITX2, DSP, DLD, SLC25A4, FOXRED1, CRYAB, RAF1, OPA3, MTO1, MRPL3, LIAS, AGK, DNM1L, TMEM70, FAH, IDH2, CAVIN1, MRPS22, SLC25A3, TSFM, DNAJC19, GFM1, COQ2, SCO2, PDHA1, TAZ, PHKA1, COX15, SURF1, GUSB, MLYCD, FXN, COX6B1, SLC22A5, PMM2, ALMS1, ZFHX3, SDHA, DOLK, BRAF, DMD, GLA, HRAS, KRAS, LDLR, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, FKTN, SGCA, SGCB, CAPN3, LMNA, PSEN2, FKRP, CAV3, NF1, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, BSCL2, BAG3, FHL1, MYBPC3, ACTA1, SYNE1, TMEM43, SYNE2, EMD, TCAP, SGCD, KCNJ2, KCND3, LAMA2, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, CACNA1D, KCNE1, KCNQ1, CACNA1C, CTNNB1, LZTR1, LAMP2, SPRED1, RASA2, RRAS, A2ML1, NOTCH1, MYH11, TRPM4, SLMAP, KCNJ8, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, SNTA1, CASQ2, AKAP9, SCN4B, KCNK3, KCNA5, PDLIM3, ILK, NEBL, ACTC1, MYLK2, TGFB3, LAMA4, PRDM16, NKX2-5, ANKRD1, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, JUP, MYPN, RANGRF, TPM1, TNNT2, GATAD1, JPH2, MYOZ2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, DTNA, TOR1AIP1, SPEG, VCL, NOS1AP, TBX5, GJA1, FHL2, OBSCN, TXNRD2, TMPO, GATA4, GATA6, XK, COL7A1, NPPA, GJA5, AGPAT2, ANK3, OBSL1, FGF12, COA5, SCN10A, CTNNA3, KCNE5, GATA5, CHRM2, CAVIN4, TBX20, MIB1, CALR3, CALM3, TNNI3K, PKP4, KLF10, TRIM63, COA6, KCND2, MRPL44, NKX2-6, FOXD4, FHOD3, PERP, PPP1R13L, KCNK17, IRX3, MYOM1, NNT, GREM2	
Specificity
1 %
 
Genes
100 %
 | 
| Hypertrophic cardiomyopathy extended panel. 
 By Health in Code in Spain.
 
TTR, AARS2, ACAD9, AGL, ACADVL, ATP5F1E, ATPAF2, GAA, ELAC2, GNPTAB, GLB1, DSP, DLD, SLC25A4, FOXRED1, CRYAB, RAF1, MTO1, MRPL3, LIAS	, (...)
View the complete list with 84 more genes 
TTR, AARS2, ACAD9, AGL, ACADVL, ATP5F1E, ATPAF2, GAA, ELAC2, GNPTAB, GLB1, DSP, DLD, SLC25A4, FOXRED1, CRYAB, RAF1, MTO1, MRPL3, LIAS, AGK, TMEM70, FAH, IDH2, MRPS22, SLC25A3, TSFM, GFM1, COQ2, SCO2, PDHA1, TAZ, PHKA1, COX15, SURF1, GUSB, MLYCD, FXN, COX6B1, SLC22A5, PMM2, BRAF, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, MAP2K2, LMNA, CAV3, NF1, TTN, DES, MYH7, FLNC, LDB3, BSCL2, BAG3, FHL1, MYBPC3, ACTA1, TCAP, LZTR1, LAMP2, KCNJ8, ANK2, RYR2, CASQ2, PDLIM3, ACTC1, MYLK2, ANKRD1, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, MYPN, TPM1, TNNT2, JPH2, MYOZ2, ACTN2, CSRP3, MYL2, MYL3, VCL, FHL2, OBSCN, AGPAT2, OBSL1, COA5, CAVIN4, CALR3, KLF10, TRIM63, COA6, MRPL44, FHOD3, MYOM1	
Specificity
1 %
 
Genes
100 %
 | 
| Resctrictive cardiomyopathy. 
 By Health in Code in Spain.
 
HFE, TTR, GLA, LMNA, TTN, DES, MYH7, FLNC, BAG3, FHL1, MYBPC3, ACTC1, TNNC1, TNNI3, MYPN, TPM1, TNNT2, ACTN2, MYL2, MYL3
 
Specificity
5 %
 
Genes
100 %
 | 
| 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 
HFE, TTR, AARS2, ACAD9, AGL, ACADVL, ATP5F1E, ATPAF2, GAA, ELAC2, PSEN1, EYA4, GNPTAB, GLB1, DSP, DLD, SLC25A4, FOXRED1, CRYAB, RAF1, OPA3, MTO1, MRPL3, LIAS, AGK, DNM1L, TMEM70, FAH, IDH2, MRPS22, SLC25A3, TSFM, DNAJC19, GFM1, COQ2, SCO2, PDHA1, TAZ, PHKA1, COX15, SURF1, GUSB, MLYCD, FXN, COX6B1, SLC22A5, PMM2, ALMS1, SDHA, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, FKTN, SGCA, SGCB, LMNA, PSEN2, FKRP, CAV3, NF1, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, BSCL2, BAG3, FHL1, MYBPC3, ACTA1, SYNE1, TMEM43, SYNE2, EMD, TCAP, SGCD, KCNJ2, LAMA2, KCNH2, HCN4, SCN5A, KCNQ1, CTNNB1, LZTR1, LAMP2, SPRED1, RASA2, RRAS, A2ML1, NOTCH1, KCNJ8, ABCC9, PKP2, ANK2, RYR2, CASQ2, PDLIM3, ILK, NEBL, ACTC1, MYLK2, TGFB3, LAMA4, PRDM16, NKX2-5, ANKRD1, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, JUP, MYPN, TPM1, TNNT2, GATAD1, JPH2, MYOZ2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, DTNA, TOR1AIP1, SPEG, VCL, FHL2, OBSCN, TXNRD2, TMPO, GATA4, GATA6, XK, COL7A1, AGPAT2, OBSL1, COA5, CTNNA3, GATA5, CHRM2, CAVIN4, TBX20, MIB1, CALR3, TNNI3K, PKP4, KLF10, TRIM63, COA6, MRPL44, FOXD4, FHOD3, PERP, PPP1R13L, MYOM1, NNT	
Specificity
1 %
 
Genes
100 %
 | 
| 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 
DSP, LMNA, CAV3, TTN, DES, FLNC, TMEM43, EMD, KCNJ2, KCNH2, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, ABCC9, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, CASQ2, KCNA5, NKX2-5, TNNI3, PRKAG2, PLN, DSG2, JUP, TNNT2, RBM20, ACTN2, DSC2, CALM3, MYL4	
Specificity
3 %
 
Genes
100 %
 | 
| 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 
TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, GLA, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, KCNJ2, KCNH2, HCN4, SCN5A, KCNE1, KCNQ1, CACNA1C, LAMP2, ABCC9, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, CASQ2, KCNA5, ACTC1, TGFB3, NKX2-5, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL, CALM3, MYL4	
Specificity
2 %
 
Genes
100 %
 | 
| 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
100 %
 | 
| 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 
TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, GLA, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, HCN4, SCN5A, CACNA1C, LAMP2, ABCC9, PKP2, RYR2, ACTC1, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
TTR, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, BAG3, MYBPC3, TMEM43, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, PKP2, RYR2, ACTC1, TNNC1, TNNI3, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, VCL	
Specificity
3 %
 
Genes
100 %
 | 
| Invitae Comprehensive Neuromuscular Disorders Panel. 
 By Invitae in United States.
 
GAA, CPT2, GNE, TRIM32, CRYAB, VCP, DPM3, PNPLA2, DPM1, ALG2, SQSTM1, TAZ, CHAT, DPAGT1, DMD, SMN1, CHRNE, DOK7, FKTN, NEB	, (...)
View the complete list with 84 more genes 
GAA, CPT2, GNE, TRIM32, CRYAB, VCP, DPM3, PNPLA2, DPM1, ALG2, SQSTM1, TAZ, CHAT, DPAGT1, DMD, SMN1, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, DNM2, LMNA, SMN2, CLCN1, FKRP, CAV3, DYSF, SCN4A, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, ATP2A1, BAG3, FHL1, SELENON, CACNA1S, RYR1, KLHL40, TPM3, ACTA1, CCDC78, MEGF10, KBTBD13, CNTN1, CFL2, TPM2, MYH2, TNNT1, MTM1, BIN1, EMD, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, KCNJ2, COLQ, MUSK, GFPT1, AGRN, CHRNA1, CHRND, CHRNB1, LAMA2, B4GAT1, DPM2, POMGNT2, CHKB, COL6A2, RXYLT1, COL6A3, LARGE1, COL6A1, B3GALNT2, ITGA7, LAMP2, FKBP14, MYPN, MYL2, KLHL41, TNPO3, POMK, STAC3, LMOD3, GMPPB, STIM1, VMA21	
Specificity
1 %
 
Genes
100 %
 | 
| Invitae Myofibrillar Myopathy Panel. 
 By Invitae in United States.
 
CRYAB, DES, FLNC, MYOT, LDB3, BAG3, FHL1, DNAJB6
 
Specificity
13 %
 
Genes
100 %
 | 
| Invitae Distal Myopathy Panel. 
 By Invitae in United States.
 
GNE, CRYAB, VCP, SQSTM1, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, BAG3, FHL1, DNAJB6
 
Specificity
6 %
 
Genes
100 %
 | 
| 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 
TTR, AGL, GAA, EYA4, CPT2, GNE, TRIM32, DSP, CRYAB, RAF1, VCP, DPM3, PNPLA2, DPM1, SQSTM1, TAZ, SLC22A5, DOLK, DMD, GLA, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, DNM2, LMNA, FKRP, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, MATR3, ATP2A1, BAG3, FHL1, SELENON, RYR1, MYBPC3, KLHL40, TPM3, ACTA1, CCDC78, MEGF10, KBTBD13, CNTN1, CFL2, TPM2, TNNT1, MTM1, BIN1, TMEM43, EMD, TRAPPC11, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, LAMA2, B4GAT1, DPM2, POMGNT2, CHKB, COL6A2, RXYLT1, COL6A3, LARGE1, COL6A1, B3GALNT2, ITGA7, HCN4, SCN5A, CACNA1C, LAMP2, FKBP14, ABCC9, PKP2, RYR2, ACTC1, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, MYPN, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, KLHL41, TNPO3, POMK, STAC3, LMOD3, GMPPB, VCL, STIM1	
Specificity
1 %
 
Genes
100 %
 | 
| Invitae Comprehensive Myopathy Panel. 
 By Invitae in United States.
 
CPT2, GNE, CRYAB, VCP, SQSTM1, NEB, DNM2, LMNA, CAV3, DYSF, SCN4A, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3	, (...)
View the complete list with 30 more genes 
CPT2, GNE, CRYAB, VCP, SQSTM1, NEB, DNM2, LMNA, CAV3, DYSF, SCN4A, TTN, DES, MYH7, FLNC, ANO5, MYOT, TIA1, LDB3, MATR3, ATP2A1, BAG3, FHL1, SELENON, CACNA1S, RYR1, KLHL40, TPM3, ACTA1, CCDC78, MEGF10, KBTBD13, CNTN1, CFL2, TPM2, TNNT1, MTM1, BIN1, DNAJB6, KCNJ2, COL6A2, COL6A3, COL6A1, FKBP14, MYPN, MYL2, KLHL41, STAC3, LMOD3, STIM1	
Specificity
2 %
 
Genes
100 %
 | 
| Invitae Hypertrophic Cardiomyopathy Panel. 
 By Invitae in United States.
 
TTR, AGL, GAA, GLA, CAV3, DES, MYH7, FLNC, BAG3, FHL1, MYBPC3, TCAP, CACNA1C, LAMP2, ACTC1, TNNC1, TNNI3, PRKAG2, PLN, TPM1	, (...)
View the complete list with 6 more genes 
TTR, AGL, GAA, GLA, CAV3, DES, MYH7, FLNC, BAG3, FHL1, MYBPC3, TCAP, CACNA1C, LAMP2, ACTC1, TNNC1, TNNI3, PRKAG2, PLN, TPM1, TNNT2, ACTN2, CSRP3, MYL2, MYL3, VCL	
Specificity
4 %
 
Genes
100 %
 | 
| Myofibrillar myopathy. 
 By GENETAQ Molecular Genetics Centre and Diagnosis of Rare Diseases in Spain.
 
TRIM32, CRYAB, LMNA, TTN, DES, MYH7, FLNC, MYOT, LDB3, BAG3, FHL1, TPM3, DNAJB6
 
Specificity
8 %
 
Genes
100 %
 | 
| Expanded Neuromuscular Disorders: Sequencing Panel. 
 By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.
 
GAA, GNE, TRIM32, CRYAB, CAVIN1, CHAT, PYGM, PMM2, DMD, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, DNM2	, (...)
View the complete list with 58 more genes 
GAA, GNE, TRIM32, CRYAB, CAVIN1, CHAT, PYGM, PMM2, DMD, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, DNM2, LMNA, PABPN1, FKRP, CAV3, DYSF, SCN4A, SGCE, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, BSCL2, BAG3, FHL1, SELENON, RYR1, TPM3, ACTA1, CFL2, TPM2, MYH2, TNNT1, MTM1, BIN1, VRK1, IGHMBP2, SYNE1, EMD, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, COLQ, MUSK, CHRNA1, CHRND, CHRNB1, SIL1, LAMA2, COL6A2, COL6A3, LARGE1, COL6A1, ITGA7, CHRNG, RYR2, PLEKHG5, AMPD1, GLE1, TNNI2, MTMR14, AMPD3	
Specificity
2 %
 
Genes
100 %
 | 
| Limb-Girdle Muscular Dystrophy: Sequencing and Deletion/Duplication Panel. 
 By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.
 
GAA, GNE, TRIM32, VCP, DMD, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT	, (...)
View the complete list with 14 more genes 
GAA, GNE, TRIM32, VCP, DMD, FKTN, SGCA, SGCB, POMGNT1, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, TTN, DES, FLNC, ANO5, MYOT, FHL1, SYNE1, SYNE2, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, SMCHD1, COL6A2, COL6A3, COL6A1	
Specificity
3 %
 
Genes
100 %
 | 
| Expanded Neuromuscular Disorders: Deletion/Duplication Panel. 
 By EGL Genetic Diagnostics Eurofins Clinical Diagnostics in United States.
 
GAA, GNE, TRIM32, CRYAB, CAVIN1, CHAT, PYGM, PMM2, DMD, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, DNM2	, (...)
View the complete list with 57 more genes 
GAA, GNE, TRIM32, CRYAB, CAVIN1, CHAT, PYGM, PMM2, DMD, CHRNE, DOK7, FKTN, NEB, SGCA, SGCB, POMGNT1, SGCG, CAPN3, RAPSN, DNM2, LMNA, PABPN1, FKRP, CAV3, DYSF, SCN4A, SGCE, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, BSCL2, BAG3, FHL1, SELENON, RYR1, TPM3, ACTA1, CFL2, TPM2, MYH2, TNNT1, MTM1, BIN1, VRK1, IGHMBP2, SYNE1, EMD, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, COLQ, MUSK, CHRNA1, CHRND, CHRNB1, SIL1, LAMA2, COL6A2, COL6A3, LARGE1, COL6A1, ITGA7, CHRNG, RYR2, PLEKHG5, AMPD1, GLE1, TNNI2, MTMR14	
Specificity
2 %
 
Genes
100 %
 | 
| Distal Hereditary Myopathy NGS Panel. 
 By Fulgent Genetics Fulgent Genetics in United States.
 
GNE, CRYAB, VCP, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, LDB3, MATR3, FHL1, TCAP
 
Specificity
8 %
 
Genes
100 %
 | 
| Myofibrillar Myopathy NGS Panel. 
 By Fulgent Genetics Fulgent Genetics in United States.
 
CRYAB, DES, FLNC, MYOT, LDB3, BAG3, FHL1, DNAJB6
 
Specificity
13 %
 
Genes
100 %
 | 
| FLNC. 
 By Fulgent Genetics Fulgent Genetics in United States.
 
FLNC
 
Specificity
100 %
 
Genes
100 %
 | 
| 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 
HFE, TTR, AARS2, ACAD9, AGL, ACADVL, GAA, ELAC2, CPT2, GLB1, TRIM32, DSP, SLC25A4, FOXRED1, NDUFAF2, CRYAB, HADHA, RAF1, VCP, MTO1, AGK, TMEM70, PNPLA2, TSFM, DNAJC19, GFM1, PCCB, PCCA, SCO2, TAZ, COX15, GUSB, MLYCD, GBE1, ETFB, ETFA, ETFDH, FXN, SLC22A5, SLC25A20, ALMS1, SDHA, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, FKTN, SGCA, SGCB, SGCG, CAPN3, LMNA, FKRP, DYSF, NF1, SCNN1G, SCNN1B, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, BAG3, FHL1, SELENON, MYBPC3, ACTA1, TMEM43, EMD, PLEC, TCAP, SGCD, ISPD, SMCHD1, LAMA2, LARGE1, HCN4, SCN5A, EEF1A2, VPS13A, LZTR1, LAMP2, SPRED1, RASA2, RRAS, ABCC6, ABCC9, PKP2, RYR2, CASQ2, ACTC1, TGFB3, PRDM16, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, JUP, MYPN, TPM1, TNNT2, GATAD1, JPH2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, DTNA, TOR1AIP1, SPEG, GMPPB, VCL, TBX5, PPP1CB, DBH, APOA1, GATA6, XK, EPG5, CTNNA3, RBCK1, TBX20, ALPK3, CALR3, TAB2, TNNI3K, MYL4, GTPBP3, RMND1, FOXD4, HAND1, CDH2, MYBPHL, FBXO32, LRRC10, PPA2, PLEKHM2	
Specificity
1 %
 
Genes
100 %
 | 
| Comprehensive Muscular Dystrophy / Myopathy Panel. 
 By Blueprint Genetics in Finland.
 
GAA, TRIM32, POLG, CRYAB, PNPLA2, SEPT9, DMD, FKTN, NEB, SGCA, SGCB, SGCG, CAPN3, LMNA, PABPN1, FKRP, CAV3, DYSF, TTN, DES	, (...)
View the complete list with 53 more genes 
GAA, TRIM32, POLG, CRYAB, PNPLA2, SEPT9, DMD, FKTN, NEB, SGCA, SGCB, SGCG, CAPN3, LMNA, PABPN1, FKRP, CAV3, DYSF, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, ATP2A1, BAG3, FHL1, SELENON, KLHL40, TPM3, ACTA1, MEGF10, KBTBD13, CFL2, TPM2, TNNT1, MTM1, SYNE1, TMEM43, EMD, TRAPPC11, DNAJB6, POMT1, TCAP, SGCD, ISPD, SMCHD1, LAMA2, POMGNT2, COL6A2, COL6A3, LARGE1, COL6A1, B3GALNT2, ITGA7, COL4A1, VPS13A, MME, COL12A1, KLHL41, LIMS2, TNPO3, TOR1AIP1, SPEG, LMOD3, GMPPB, MICU1, POGLUT1, RBCK1, COL4A2, VMA21, TMEM126B	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
DSP, RAF1, DMD, LMNA, TTN, DES, MYH7, FLNC, BAG3, MYBPC3, EMD, TCAP, HCN4, SCN5A, LAMP2, ABCC9, PKP2, RYR2, MYH6, PLN, DSG2, JUP, TPM1, TNNT2, JPH2, RBM20, DSC2, DTNA, VCL, CTNNA3, FBXO32, PLEKHM2	
Specificity
4 %
 
Genes
100 %
 | 
| 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 
HFE, TTR, AARS2, ACAD9, AGL, ACADVL, GAA, ELAC2, CPT2, GLB1, TRIM32, DSP, SLC25A4, FOXRED1, NDUFAF2, CRYAB, HADHA, RAF1, VCP, MTO1, AGK, TMEM70, PNPLA2, TSFM, DNAJC19, GFM1, PCCB, PCCA, SCO2, TAZ, COX15, GUSB, MLYCD, GBE1, ETFB, ETFA, ETFDH, FXN, SLC22A5, SLC25A20, ALMS1, SDHA, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, FKTN, SGCA, SGCB, SGCG, CAPN3, LMNA, FKRP, CAV3, DYSF, NF1, SCNN1G, SCNN1B, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, BAG3, FHL1, SELENON, MYBPC3, ACTA1, TMEM43, EMD, PLEC, POMT1, TCAP, SGCD, ISPD, SMCHD1, KCNJ2, LAMA2, LARGE1, KCNH2, SCN1B, HCN4, SCN5A, CACNA2D1, EEF1A2, VPS13A, KCNE1, KCNQ1, CACNA1C, LZTR1, LAMP2, SPRED1, RASA2, RRAS, ACTA2, ABCC6, TRPM4, ABCC9, SCN3B, CACNB2, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, KCNJ5, CASQ2, AKAP9, KCNA5, ACTC1, TGFB3, PRDM16, NKX2-5, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, JUP, MYPN, TPM1, TNNT2, GATAD1, JPH2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, DTNA, TOR1AIP1, SPEG, GMPPB, VCL, NOS1AP, SALL4, TBX5, PPP1CB, DBH, APOA1, GATA6, XK, EPG5, NUP155, ENPP1, SCN10A, CTNNA3, RBCK1, GATA5, TBX20, ALPK3, CALR3, CALM3, TAB2, TNNI3K, MYL4, GTPBP3, RMND1, TECRL, FOXD4, HAND1, CDH2, MYBPHL, FBXO32, LRRC10, PPA2, PLEKHM2	
Specificity
1 %
 
Genes
100 %
 | 
| 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 
TTR, GLB1, DSP, RAF1, PCCB, PCCA, TAZ, MLYCD, GBE1, ETFB, ETFA, ETFDH, ALMS1, DOLK, DMD, FKTN, LMNA, DYSF, TTN, DES, MYH7, FLNC, BAG3, MYBPC3, ACTA1, EMD, TCAP, HCN4, SCN5A, EEF1A2, VPS13A, LAMP2, ABCC6, ABCC9, PKP2, ACTC1, PRDM16, TNNC1, TNNI3, MYH6, PLN, DSG2, JUP, TPM1, TNNT2, JPH2, RBM20, ACTN2, DSC2, TOR1AIP1, SPEG, VCL, TBX5, APOA1, GATA6, EPG5, RBCK1, TBX20, ALPK3, TAB2, TNNI3K, MYL4, RMND1, FOXD4, HAND1, MYBPHL, GATAD2A, FBXO32, LRRC10, PLEKHM2	
Specificity
2 %
 
Genes
100 %
 | 
| Hypertrophic Cardiomyopathy (HCM) Panel. 
 By Blueprint Genetics in Finland.
 
TTR, ACAD9, AGL, ACADVL, GAA, ELAC2, SLC25A4, NDUFAF2, RAF1, AGK, COX15, FXN, BRAF, GLA, HRAS, SOS1, CBL, MYH7, FLNC, BAG3	, (...)
View the complete list with 18 more genes 
TTR, ACAD9, AGL, ACADVL, GAA, ELAC2, SLC25A4, NDUFAF2, RAF1, AGK, COX15, FXN, BRAF, GLA, HRAS, SOS1, CBL, MYH7, FLNC, BAG3, FHL1, MYBPC3, ACTA1, LAMP2, ABCC9, ACTC1, TNNI3, PRKAG2, TPM1, TNNT2, JPH2, ACTN2, CSRP3, MYL2, MYL3, APOA1, EPG5, ALPK3	
Specificity
3 %
 
Genes
100 %
 | 
| Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC) Panel. 
 By Blueprint Genetics in Finland.
 
DSP, LMNA, TTN, DES, MYH7, FLNC, LDB3, TMEM43, PKP2, RYR2, TGFB3, PLN, DSG2, JUP, DSC2, CTNNA3, CDH2
 
Specificity
6 %
 
Genes
100 %
 | 
| Genetic Study of Hypertrophic Cardiomyopathy Panel (2 panels: 57 genes or 18 genes). 
 By HeartGenetics, Genetics and Biotechnology, SA in Portugal.
 
CRYAB, BRAF, MYH7, FLNC, LDB3, FHL1, MYBPC3, TCAP, LAMP2, ACTC1, TNNC1, TNNI3, TPM1, TNNT2, CSRP3, MYL2, MYL3
 
Specificity
6 %
 
Genes
100 %
 | 
| Myopathy, myofibrillar, 5. 
 By Bioarray in Spain.
 
FLNC
 
Specificity
100 %
 
Genes
100 %
 | 
| 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 
PSEN1, EYA4, DSP, CRYAB, RAF1, MRPL3, TAZ, DMD, FKTN, LMNA, PSEN2, TTN, DES, MYH7, FLNC, LDB3, BAG3, MYBPC3, TCAP, SGCD, HCN4, SCN5A, LAMP2, ABCC9, ACTC1, MYLK2, LAMA4, PRDM16, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, DSG2, MYPN, TPM1, TNNT2, GATAD1, JPH2, MYOZ2, RBM20, ACTN2, CSRP3, MYL2, MYL3, DTNA, VCL, TBX5, GATA6, TBX20, MIB1, CALR3	
Specificity
2 %
 
Genes
100 %
 | 
| MYOFIBRILLAR MYOPATHY. 
 By Laboratorio de Genetica Clinica SL in Spain.
 
CRYAB, DES, FLNC, MYOT, LDB3, BAG3
 
Specificity
17 %
 
Genes
100 %
 | 
| Filaminopathy , Sequencing FLNC Gene. 
 By Reference Laboratory Genetics in Spain.
 
FLNC
 
Specificity
100 %
 
Genes
100 %
 | 
| Familial Hypertrophic Cardiomyopathy, Panel Massive Sequencing (NGS) 37 Genes. 
 By Reference Laboratory Genetics in Spain.
 
TTR, AGL, GAA, SLC25A4, FXN, GLA, PTPN11, CAV3, TTN, DES, MYH7, FLNC, LDB3, MYBPC3, TCAP, LAMP2, ANK2, RYR2, ACTC1, MYLK2	, (...)
View the complete list with 17 more genes 
TTR, AGL, GAA, SLC25A4, FXN, GLA, PTPN11, CAV3, TTN, DES, MYH7, FLNC, LDB3, MYBPC3, TCAP, LAMP2, ANK2, RYR2, ACTC1, MYLK2, TNNC1, TNNI3, MYH6, PRKAG2, PLN, NEXN, MYPN, TPM1, TNNT2, JPH2, MYOZ2, ACTN2, CSRP3, MYL2, MYL3, VCL, CALR3	
Specificity
3 %
 
Genes
100 %
 | 
| Restrictive Cardiomyopathy , Panel Massive Sequencing (NGS) 4 Genes. 
 By Reference Laboratory Genetics in Spain.
 
FLNC, TNNI3, MYPN, TNNT2
 
Specificity
25 %
 
Genes
100 %
 | 
| Myofibrillar Myopathy, Panel Massive Sequencing (NGS) 8 Genes. 
 By Reference Laboratory Genetics in Spain.
 
CRYAB, DES, FLNC, MYOT, LDB3, BAG3, FHL1, DNAJB6
 
Specificity
13 %
 
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 
ACADM, DSP, LMNA, CAV3, TTN, DES, FLNC, TMEM43, KCNJ2, KCND3, KCNH2, SCN1B, HCN4, SCN5A, CACNA1D, KCNE1, KCNQ1, CACNA1C, LAMP2, TRPM4, ABCC9, SCN2B, SCN3B, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, TRDN, KCNE2, KCNJ5, SNTA1, CASQ2, AKAP9, SCN4B, TGFB3, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TNNT2, DSC2, SCN10A, CTNNA3	
Specificity
3 %
 
Genes
100 %
 | 
| Muscle Polyneuropathies , Panel Massive Sequencing (NGS) 111 Genes. 
 By Reference Laboratory Genetics in Spain.
 
GAA, GNE, TRIM32, CRYAB, VCP, CAVIN1, DPM3, PNPLA2, DPM1, PHKA1, CHAT, PYGM, PMM2, DMD, CHRNE, DOK7, FKTN, NEB, PEX2, PEX7	, (...)
View the complete list with 91 more genes 
GAA, GNE, TRIM32, CRYAB, VCP, CAVIN1, DPM3, PNPLA2, DPM1, PHKA1, CHAT, PYGM, PMM2, DMD, CHRNE, DOK7, FKTN, NEB, PEX2, PEX7, SGCA, SGCB, PEX1, POMGNT1, SGCG, CAPN3, RAPSN, TRPV4, DNM2, LMNA, CLCN1, PABPN1, FKRP, CAV3, UBA1, DYSF, SCN4A, TOR1A, SGCE, TTN, DES, MYH7, FLNC, ANO5, MYOT, LDB3, ATP2A1, BSCL2, BAG3, FHL1, SELENON, CACNA1S, RYR1, TPM3, ACTA1, MEGF10, KBTBD13, CNTN1, CFL2, TPM2, MYH2, TNNT1, MTM1, BIN1, DYNC1H1, VRK1, IGHMBP2, SYNE1, TMEM43, SYNE2, EMD, DNAJB6, DAG1, PLEC, POMT2, POMT1, TCAP, SGCD, ISPD, COLQ, MUSK, CHRNA1, CHRND, CHRNB1, SIL1, LAMA2, CHKB, COL6A2, COL6A3, LARGE1, COL6A1, ITGA7, PEX6, CACNA1C, PEX14, PEX3, PEX26, PEX10, PEX12, PEX5, CHRNG, LAMP2, RYR2, PLEKHG5, AMPD1, GLE1, TNNI2, MTMR14, TNNT3, PEX11B, AMPD3	
Specificity
1 %
 
Genes
100 %
 | 
| 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 
TTR, ACADVL, EYA4, CPT2, DSP, CRYAB, RAF1, TMEM70, DNAJC19, TAZ, SLC22A5, ALMS1, SDHA, DOLK, DMD, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, LDB3, BAG3, MYBPC3, TMEM43, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, PKP2, RYR2, ACTC1, TNNC1, TNNI3, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, VCL	
Specificity
3 %
 
Genes
100 %
 | 
| 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 
TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, GLA, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, HCN4, SCN5A, CACNA1C, LAMP2, ABCC9, PKP2, RYR2, ACTC1, TGFB3, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
TTR, AGL, ACADVL, GAA, ELAC2, EYA4, CPT2, DSP, CRYAB, RAF1, MTO1, TMEM70, DNAJC19, TAZ, SLC22A5, ALMS1, SDHA, DOLK, DMD, GLA, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, HCN4, SCN5A, CACNA1C, LAMP2, ABCC9, PKP2, RYR2, ACTC1, TGFB3, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, FKTN, LMNA, FKRP, CAV3, NF1, TTN, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, HCN4, SCN5A, CACNA1C, RASA1, LAMP2, SPRED1, RRAS, A2ML1, ABCC9, PKP2, RYR2, ACTC1, TGFB3, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, GLA, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, KCNJ2, KCNH2, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, LAMP2, ABCC9, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, SNTA1, CASQ2, SCN4B, ACTC1, TGFB3, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL, SCN10A, CALM3	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
TTR, AGL, GAA, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, FKTN, LMNA, FKRP, CAV3, NF1, TTN, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, KCNJ2, KCNH2, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, RASA1, LAMP2, SPRED1, RRAS, A2ML1, ABCC9, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, SNTA1, CASQ2, SCN4B, ACTC1, TGFB3, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL, SCN10A, CALM3	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
TTR, AGL, ACADVL, GAA, ELAC2, EYA4, CPT2, DSP, CRYAB, RAF1, MTO1, TMEM70, DNAJC19, TAZ, SLC22A5, ALMS1, SDHA, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, FKTN, LMNA, FKRP, CAV3, NF1, TTN, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, KCNJ2, KCNH2, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, RASA1, LAMP2, SPRED1, RRAS, A2ML1, ABCC9, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, SNTA1, CASQ2, SCN4B, ACTC1, TGFB3, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL, SCN10A, CALM3	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
TTR, AGL, ACADVL, GAA, ELAC2, EYA4, CPT2, DSP, CRYAB, RAF1, MTO1, TMEM70, DNAJC19, TAZ, SLC22A5, ALMS1, SDHA, DOLK, BRAF, DMD, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, FKTN, LMNA, FKRP, CAV3, NF1, TTN, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, HCN4, SCN5A, CACNA1C, RASA1, LAMP2, SPRED1, RRAS, A2ML1, ABCC9, PKP2, RYR2, ACTC1, TGFB3, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL	
Specificity
2 %
 
Genes
100 %
 | 
| 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 
TTR, AGL, ACADVL, GAA, ELAC2, EYA4, CPT2, DSP, CRYAB, RAF1, MTO1, TMEM70, DNAJC19, TAZ, SLC22A5, ALMS1, SDHA, DOLK, DMD, GLA, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TMEM43, EMD, TCAP, SGCD, KCNJ2, KCNH2, HCN4, SCN5A, CACNA2D1, KCNE1, KCNQ1, CACNA1C, LAMP2, ABCC9, KCNE3, CACNB2, GPD1L, PKP2, ANK2, RYR2, CALM1, CALM2, TRDN, KCNE2, SNTA1, CASQ2, SCN4B, ACTC1, TGFB3, TNNC1, TNNI3, PRKAG2, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, MYL2, MYL3, VCL, SCN10A, CALM3	
Specificity
2 %
 
Genes
100 %
 | 
| Phosphorus Hypertrophic Cardiomyopathy Including Rasopathies and Recessive Pediatric Syndromes Panel. 
 By Phosphorus Diagnostics LLC in United States.
 
TTR, AGL, ACADVL, GAA, ELAC2, CPT2, RAF1, MTO1, BRAF, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2	, (...)
View the complete list with 29 more genes 
TTR, AGL, ACADVL, GAA, ELAC2, CPT2, RAF1, MTO1, BRAF, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, CAV3, NF1, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TCAP, CACNA1C, RASA1, LAMP2, SPRED1, RRAS, A2ML1, ACTC1, TNNC1, TNNI3, PRKAG2, PLN, TPM1, TNNT2, ACTN2, CSRP3, MYL2, MYL3, VCL	
Specificity
3 %
 
Genes
100 %
 | 
| Phosphorus Hypertrophic Cardiomyopathy Panel. 
 By Phosphorus Diagnostics LLC in United States.
 
TTR, AGL, GAA, GLA, CAV3, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TCAP, CACNA1C, LAMP2, ACTC1, TNNC1, TNNI3, PRKAG2, PLN	, (...)
View the complete list with 7 more genes 
TTR, AGL, GAA, GLA, CAV3, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TCAP, CACNA1C, LAMP2, ACTC1, TNNC1, TNNI3, PRKAG2, PLN, TPM1, TNNT2, ACTN2, CSRP3, MYL2, MYL3, VCL	
Specificity
4 %
 
Genes
100 %
 | 
| 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 
TTR, EYA4, DSP, CRYAB, RAF1, TAZ, SLC22A5, DOLK, DMD, FKTN, LMNA, FKRP, CAV3, TTN, DES, MYH7, FLNC, LDB3, BAG3, MYBPC3, TMEM43, EMD, TCAP, SGCD, SCN5A, LAMP2, ABCC9, PKP2, RYR2, ACTC1, TNNC1, TNNI3, PLN, DSG2, JUP, TPM1, TNNT2, RBM20, ACTN2, CSRP3, DSC2, VCL	
Specificity
3 %
 
Genes
100 %
 | 
| Phosphorus Hypertrophic Cardiomyopathy Including Rasopathies Panel. 
 By Phosphorus Diagnostics LLC in United States.
 
TTR, AGL, GAA, RAF1, BRAF, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, CAV3, NF1, DES	, (...)
View the complete list with 25 more genes 
TTR, AGL, GAA, RAF1, BRAF, GLA, HRAS, KRAS, MAP2K1, NRAS, PTPN11, SHOC2, SOS1, SOS2, RIT1, MAP2K2, CBL, CAV3, NF1, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TCAP, CACNA1C, RASA1, LAMP2, SPRED1, RRAS, A2ML1, ACTC1, TNNC1, TNNI3, PRKAG2, PLN, TPM1, TNNT2, ACTN2, CSRP3, MYL2, MYL3, VCL	
Specificity
3 %
 
Genes
100 %
 | 
| Phosphorus Hypertrophic Cardiomyopathy Including Recessive Pediatric Syndromes Panel. 
 By Phosphorus Diagnostics LLC in United States.
 
TTR, AGL, ACADVL, GAA, ELAC2, CPT2, MTO1, GLA, CAV3, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TCAP, CACNA1C, LAMP2, ACTC1	, (...)
View the complete list with 11 more genes 
TTR, AGL, ACADVL, GAA, ELAC2, CPT2, MTO1, GLA, CAV3, DES, MYH7, FLNC, LDB3, BAG3, FHL1, MYBPC3, TCAP, CACNA1C, LAMP2, ACTC1, TNNC1, TNNI3, PRKAG2, PLN, TPM1, TNNT2, ACTN2, CSRP3, MYL2, MYL3, VCL	
Specificity
4 %
 
Genes
100 %
 |