Risk of heart disease often runs in families, suggesting a genetic influence. Genetic testing allows us to look at your DNA to identify any differences that could predispose you to developing certain health problems. In some cases genetic testing may be used to diagnose an inherited cardiac disease. However, in most cases genetic testing is used to help determine which family members could develop the heart problems that are running in the family and which family members will not develop those heart problems. Those identified at risk of heart disease could change their lifestyle and take therapeutic measures to reduce their risk of developing the disease.

 Pan-Cardio NGS Panel

223 Genes:
A2ML1, ABCC9, ACTA2, ACTB, ACTC1, ACTN2, ACVR2B, ACVRL1, AKAP9, ALMS1, ANK2, ANKRD1, APOA5, APOB, BAG3, BBS10, BCOR, BMPR2, BRAF, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CALR3, CASQ2, CAV1, CAV3, CBL, CBS, CCDC103, CCDC39, CCDC40, CHD7, CHRM2, COL3A1, COL5A1, COL5A2, COX15, CPT1A, CRELD1, CRYAB, CSRP3, CTF1, CTNNA3, DES, DMD, DNAAF1, DNAAF2, DNAAF3, DNAAF5, DNAH11, DNAH5, DNAI1, DNAI2, DNAL1, DOLK, DSC2, DSG2, DSP, DTNA, DYX1C1, ELAC2, ELN, EMD, ENG, EYA4, FBN1, FBN2, FHL1, FHL2, FKRP, FKTN, FLNA, FOXH1, FXN, GAA, GATA4, GATA6, GATAD1, GDF1, GJA1, GJA5, GLA, GPC3, GPD1L, GYG1, HAMP, HAND1, HCN4, HFE, HFE2, HRAS, ILK, INVS, JAG1, JPH2, JUP, KAT6B, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNE5, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNK3, KCNQ1, KRAS, LAMA4, LAMP2, LDB3, LDLR, LDLRAP1, LEFTY2, LMNA, LZTR1, MAP2K1, MAP2K2, MED12, MED13L, MIB1, MKS1, MRPL3, MTO1, MURC, MYBPC3, MYH11, MYH6, MYH7, MYL2, MYL3, MYLK, MYLK2, MYOM1, MYOZ2, MYPN, NDUFAF1, NEBL, NEK8, NEXN, NF1, NKX2-5, NKX2-6, NME8, NODAL, NOTCH1, NPHP3, NPPA, NR2F2, NRAS, NSD1, OFD1, PCSK9, PDLIM3, PKP2, PLN, PLOD1, PRDM16, PRKAG2, PRKG1, PSEN2, PTPN11, RAF1, RANGRF, RASA1, RBM20, RIT1, RRAS, RYR2, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SDHA, SGCD, SHOC2, SKI, SLC25A20, SLC2A10, SLC40A1, SLMAP, SMAD3, SMAD4, SMAD6, SMAD9, SNTA1, SOS1, SOS2, SPRED1, SYNE1, TAZ, TBX1, TBX20, TBX5, TCAP, TFR2, TGFB2, TGFB3, TGFBR1, TGFBR2, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TRPM4, TTC8, TTN, TTR, TXNRD2, VCL, YWHAE, ZFPM2, ZIC3

Alagille Syndrome NGS Panel

02 Genes:
JAG1, NOTCH2

Arrhythmia NGS Panel

45 Genes:
AKAP9, ANK2, CACNA1C, CACNA2D1, CACNB2, CALM1, CASQ2, CAV3, CPT1A, DES, DSC2, DSG2, DSP, GJA5, GPD1L, GYG1, HCN4, JUP, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ8, KCNQ1, LDB3, LMNA, NKX2-5, NPPA, PKP2, PRKAG2, RYR2, SCN1B, SCN3B, SCN4B, SCN5A, SLC25A20, SNTA1, TBX5, TGFB3, TMEM43, TRDN, TRPM4

Arrhythmogenic Right Ventricular Cardiomyopathy NGS Panel

34 Genes:
AKAP9, ANK2, CACNA1C, CACNB2, CASQ2, CAV3, DES, DSC2, DSG2, DSP, GPD1L, HCN4, JUP, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LDB3, LMNA, NKX2-5, PKP2, RANGRF, RYR2, SCN1B, SCN3B, SCN4B, SCN5A, SNTA1, TGFB3, TMEM43

Atrial Fibrillation NGS Panel

24Genes:
ABCC9, GATA4, GATA6, GJA5, HCN4, KCNA5, KCND3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LDB3, LMNA, NPPA, NUP155, RYR2, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A

15 Genes:
CACNA1C, CACNA2D1, CACNB2, GPD1L, HCN4, KCND3, KCNE3, KCNE5, KCNJ8, RANGRF, SCN1B, SCN2B, SCN3B, SCN5A, TRPM4

Cardio-Facio-Cutaneous Syndrome NGS Panel

06 Genes:
BRAF, KRAS, MAP2K1, MAP2K2, SHOC2, SOS1

Catecholaminergic Polymorphic Ventricular Tachycardia NGS Panel

09 Genes:
ANK2, CALM1, CALM2, CALM3, CASQ2, KCNJ2, KCNQ1, RYR2, TRDN

Congenital Heart Disease NGS Panel

114 Genes:
ACTC1, ACVR2B, AKT3, ALMS1, ARL6, ARMC4, B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCOR, BRAF, C21orf59, CBL, CC2D2A, CCDC103, CCDC114, CCDC151, CCDC28B, CCDC39, CCDC40, CCDC65, CCNO, CEP290, CFAP53, CFC1, CHD7, CITED2, CPS1, CRELD1, CYR61, DNAAF1, DNAAF2, DNAAF3, DNAAF5, DNAH11, DNAH5, DNAH8, DNAI1, DNAI2, DNAL1, DRC1, DTNA, DYX1C1, ELN, FLNA, FOXF1, FOXH1, GATA4, GATA6, GDF1, GJA1, GPC3, HAND1, HRAS, INVS, JAG1, KIF7, KRAS, LEFTY2, MAP2K1, MAP2K2, MCIDAS, MED13L, MKKS, MKS1, MYH6, NEK8, NKX2-5, NKX2-6, NME8, NODAL, NOTCH1, NPHP3, NR2F2, NRAS, NSD1, NTRK3, OFD1, PIK3CA, PIK3R2, PITX2, PTPN11, RAF1, RAI1, RBM10, RIT1, RPGRIP1L, SEMA3E, SHOC2, SMAD6, SOS1, SPAG1, TAB2, TBX1, TBX20, TBX5, TCTN2, TLL1, TMEM216, TMEM231, TMEM67, TRIM32, TTC8, WDPCP, ZFPM2, ZIC3, ZMYND10

Dilated Cardiomyopathy NGS Panel

56 Genes:
ABCC9, ACTC1, ACTN2, ANKRD1, BAG3, CASQ2, CAV3, CHRM2, CRYAB, CSRP3, DES, DMD, DOLK, DSC2, DSG2, DSP, DTNA, EMD, GATAD1, GLA, JUP, LAMA4, LAMP2, LDB3, LMNA, MURC, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYOZ2, MYPN, NEBL, NEXN, PKP2, PLN, PRDM16, PRKAG2, PTPN11, RAF1, RBM20, RYR2, SCN5A, SGCD, TAZ, TCAP, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TTN, TTR, VCL

Ehlers-Danlos Syndrome NGS Panel

04 Genes:
COL3A1, COL5A1, COL5A2, PLOD1

Hemiplegia/Stroke NGS Panel

10 Genes:
ATP1A2, ATP1A3, CACNA1A, COL4A1, COL4A2, NOTCH3, OTC, POLG, SCN1A, SLC2A1

Hypertrophic Cardiomyopathy NGS Panel

77 Genes:
A2ML1, ABCC9, ACTC1, ACTN2, ANKRD1, BAG3, BRAF, CALR3, CAV3, CBL, CRYAB, CSRP3, CTF1, DES, DMD, DSC2, DSG2, DSP, DTNA, ELAC2, EMD, FHL1, FKTN, GATA4, GATAD1, GLA, HRAS, ILK, JPH2, JUP, KRAS, LAMA4, LAMP2, LDB3, LMNA, MAP2K1, MAP2K2, MTO1, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOM1, MYOZ2, MYPN, NEBL, NEXN, NF1, NRAS, PDLIM3, PKP2, PLN, PRKAG2, PTPN11, RAF1, RASA1, RBM20, RIT1, RYR2, SCN5A, SGCD, SHOC2, SOS1, SPRED1, TAZ, TCAP, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL

Jervell and Lange-Nielsen Syndrome NGS Panel

02 Genes:
KCNE1, KCNQ1

Left Ventricular Noncompaction NGS Panel

24 Genes:
ACTC1, ACTN2, DSP, DTNA, HCN4, LAMP2, LDB3, LMNA, MIB1, MYBPC3, MYH7, NEXN, PLN, PRDM16, RYR2, SCN5A, TAZ, TCAP, TNNI3, TNNT2, TPM1, TTN, VCL, YWHAE

Long QT Syndrome NGS Panel

16 Genes:
AKAP9, ANK2, CACNA1C, CALM1, CALM2, CALM3, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNQ1, SCN4B, SCN5A, SNTA1

MarfanSyndrome and Thoracic Aortic Aneurysm and Dissection NGS Panel

22 Genes:
ACTA2, CBS, COL3A1, COL5A1, COL5A2, FBN1, FBN2, FLNA, MED12, MYH11, MYLK, NOTCH1, PLOD1, PRKG1, SKI, SLC2A10, SMAD3, SMAD4, TGFB2, TGFB3, TGFBR1, TGFBR2

Noonan Syndrome NGS Panel

20 Genes:
A2ML1, ACTB, ACTG1, BRAF, CBL, HRAS, KAT6B, KRAS, LZTR1, MAP2K1, MAP2K2, NRAS, PTPN11, RAF1, RIT1, RRAS, SHOC2, SOS1, SOS2, SPRED1

Short QT NGS Panel

04 Genes:
CACNA1C, KCNH2, KCNJ2, KCNQ1

Sudden Death Syndrome NGS Panel

68 Genes:
AKAP9, ANK2, CACNA1C, CACNB2, CALR3, CASQ2, CAV3, CSRP3, CTF1, DES, DSC2, DSG2, DSP, DTNA, EYA4, FBN1, FBN2, FKTN, GJA5, GPD1L, JPH2, JUP, KCNA5, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNQ1, LAMP2, LDB3, LMNA, LRP6, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYLK2, MYOZ2, NEXN, NPPA, PKP2, PLN, PRKAG2, PSEN1, PSEN2, RBM20, RYR2, SCN1B, SCN3B, SCN4B, SCN5A, SGCD, SLC25A4, SNTA1, TAZ, TCAP, TGFB3, TGFBR2, TMEM43, TMPO, TNNC1, TNNI3, TNNT2, TPM1, TTN, VCL