Cardiology

Code Test Genes TAT
8884 DCMNext ABCC9, ACTC1, ACTN2, ALMS1, ANKRD1, BAG3, CSRP3, DES, DMD, DOLK, DSP, FKRP, FLNC, LAMA4, LAMP2, LDB3, LMNA, MYBPC3, MYH6, MYH7, MYPN, NEXN, NKX2-5, PLN, RAF1, RBM20, SCN5A, TAZ, TBX20, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL 14-21 days
8902 CPVTNext CALM1, CASQ2, RYR2, TRDN 14-21 days
9520 CustomNext Cardio
CustomNext-Cardio
Other Lipid Disorders
ABCA1, ABCC9, ABCG5, ABCG8, ACTA2, ACTC1, ACTN2, ACVRL1, AKAP9, ALMS1, ALPK3, ANK2, ANKRD1, APOA1, APOA5, APOB, APOC2, APOC3, APOE, BAG3, BGN, BRAF, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, CBL, CBS, CHST14, COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, CRYAB, CSRP3, CYP27A1, DES, DMD, DOLK, DSC2, DSG2, DSP, EFEMP2, EMD, ENG, EPHB4, EYA4, FBN1, FBN2, FHL1, FKBP14, FKRP, FKTN, FLNA, FLNC, FOXE3, GAA, GATA4, GATAD1, GDF2, GLA, GPD1L, GPIHBP1, HCN4, HRAS, JAG1, JPH2, JUP, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, KRAS, LAMA4, LAMP2, LCAT, LDB3, LDLR, LDLRAP1, LIPA, LMF1, LMNA, LOX, LPL, LZTR1, MAP2K1, MAP2K2, MAT2A, MED12, MFAP5, MYBPC3, MYH11, MYH6, MYH7, MYL2, MYL3, MYLK, MYOZ2, MYPN, NEXN, NF1, NKX2-5, NOTCH1, NRAS, PCSK9, PKP2, PLN, PLOD1, PPP1CB, PRDM5, PRKAG2, PRKG1, PTPN11, RAF1, RASA1, RBM20, RIT1, RYR2, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SHOC2, SKI, SLC2A10, SLCO1B1, SMAD3, SMAD4, SNTA1, SOS1, SOS2, SPRED1, TAZ, TBX1, TBX20, TBX5, TCAP, TECRL, TGFB2, TGFB3, TGFBR1, TGFBR2, TMEM43, TNNC1, TNNI3, TNNT2, TNXB, TPM1, TRDN, TRPM4, TTN, TTR, TXNRD2, VCL, ZNF469 14-21 days
8890 LongQTNext AKAP9, ANK2, CACNA1C, CALM1, CALM2, CALM3, CAV3, KCNE1, KCNE2, KCNH2, KCNJ2, KCNJ5, KCNQ1, SCN4B, SCN5A, SNTA1, TRDN 14-21 days
8920 FCSNext APOA5, APOC2, GPIHBP1, LMF1, LPL 14-21 days
8930 Sitosterolemia ABCG5, ABCG8 14-21 days
8789 TAADNext ACTA2, BGN, CBS, CHST14, COL1A1, COL1A2, COL3A1, COL5A1, COL5A2, EFEMP2, FBN1, FBN2, FKBP14, FLNA, FOXE3, LOX, MAT2A, MED12, MFAP5, MYH11, MYLK, NOTCH1, PLOD1, PRDM5, PRKG1, SKI, SLC2A10, SMAD3, SMAD4, TGFB2, TGFB3, TGFBR1, TGFBR2, TNXB, ZNF469 14-21 days
8900 RhythmNext AKAP9, ANK2, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, DES, DSC2, DSG2, DSP, GPD1L, HCN4, JUP, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LMNA, NKX2-5, PKP2, PLN, RYR2, SCN10A, SCN1B, SCN3B, SCN4B, SCN5A, SNTA1, TBX5, TECRL, TMEM43, TRDN, TRPM4 14-21 days
8936 HCMNext ACTC1, ACTN2, ALPK3, ANKRD1, CSRP3, FHL1, FLNC, GLA, JPH2, LAMP2, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYPN, NEXN, PLN, PRKAG2, PTPN11, RAF1, RIT1, SOS1, TCAP, TNNC1, TNNI3, TNNT2, TPM1, TTR, VCL 14-21 days
8887 CMNext ABCC9, ACTC1, ACTN2, ALMS1, ALPK3, ANKRD1, BAG3, CRYAB, CSRP3, DES, DMD, DOLK, DSC2, DSG2, DSP, EMD, FHL1, FKRP, FLNC, GLA, HCN4, JPH2, JUP, LAMA4, LAMP2, LDB3, LMNA, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYPN, NEXN, NKX2-5, PKP2, PLN, PRKAG2, PTPN11, RAF1, RBM20, RIT1, RYR2, SCN5A, SOS1, TAZ, TBX20, TCAP, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR, VCL 14-21 days
8911 CardioNext ABCC9, ACTC1, ACTN2, AKAP9, ALMS1, ALPK3, ANK2, ANKRD1, BAG3, CACNA1C, CACNA2D1, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV3, CRYAB, CSRP3, DES, DMD, DOLK, DSC2, DSG2, DSP, EMD, EYA4, FHL1, FKRP, FKTN, FLNC, GATAD1, GLA, GPD1L, HCN4, JPH2, JUP, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNJ8, KCNQ1, LAMA4, LAMP2, LDB3, LMNA, MYBPC3, MYH6, MYH7, MYL2, MYL3, MYOZ2, MYPN, NEXN, NKX2-5, PKP2, PLN, PRKAG2, PTPN11, RAF1, RBM20, RIT1, RYR2, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SNTA1, SOS1, TAZ, TBX20, TBX5, TCAP, TECRL, TGFB3, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TRPM4, TTN, TTR, TXNRD2, VCL 14-21 days
8904 ARVCNext DES, DSC2, DSG2, DSP, JUP, LMNA, PKP2, PLN, RYR2, SCN5A, TMEM43 14-21 days
8680 FHNext
FHNext
Other Lipid Disorders
APOB, LDLR, LDLRAP1, PCSK9 14-21 days
8402 NoonanNext BRAF, CBL, HRAS, KRAS, LZTR1, MAP2K1, MAP2K2, NF1, NRAS, PPP1CB, PTPN11, RAF1, RASA1, RIT1, SHOC2, SOS1, SOS2, SPRED1 14-21 days

Please select a category to find your test or learn more about our highlighted tests below

why choose ambry

More than 1 in 200 people have an inherited cardiovascular condition. Ambry’s mission is to provide the most advanced genetic testing information available to help you identity those at risk and determine the best treatment options. If we know a patient has a disease-causing genetic change, not only does it mean better disease management, but it also indicates that we can test others in the family and provide them with potentially life-saving information.

Choose from one of our more frequently ordered tests listed below.

TAADNext®

Thoracic aortic aneurysms and dissections (TAAD), Marfan syndrome, and other related disorders are serious genetic conditions that often contribute to sudden cardiac death, so an accurate diagnosis is essential to prevent life-threatening events. TAADNext is a gene panel that precisely analyzes 35 genes associated with these disorders, helping you confirm a diagnosis that aids in patient management and treatment options.

FHNext®

Familial hypercholesterolemia (FH) is an inherited disorder characterized by high cholesterol and an increased risk for heart disease. FHNext is a 4-gene panel that analyzes genes associated with familial hypercholesterolemia, which can clarify a diagnosis and allow for individualized disease management and treatment.

LongQTNext®

Long QT syndrome, Brugada syndrome, and short QT syndrome are inherited arrhythmias that are often asymptomatic and can lead to sudden cardiac death. LongQTNext is a 17 gene panel that analyzes genes most commonly associated with these inherited arrhythmias. This test can be an effective way to confirm an arrhythmia disorder and direct medical management and treatment decisions.

RhythmNext®

Inherited arrhythmias such as BrS, CPVT, LQTS, and SQTS can often lead to sudden cardiac death. RhythmNext, a 42-gene panel analyzes genes associated with these arrhythmias and can be an effective way of confirming a diagnosis. At-risk individuals are identified with vital information aiding in management and intervention options for both the patient and their family.

HCMNext®

HCMNext is a multi-gene panels that can be ordered individually or on a reflex basis for patients with hypertrophic cardiomyopathy (HCM). Often, HCM can be asymptomatic and sudden death is the first and only symptom. Therefore, genetic testing may be the most effective way of identifying at-risk individuals, or confirming a diagnosis. HCMNext includes 30 genes that cause HCM. These genes make up over 80% of known genetic causes of HCM.

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