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This test is a medical examination designed to assess an individual’s risk for developing these two conditions.

Genes:
Monogenic Diabetes Panel (28 genes) ABCC8, APPL1, BLK, EIF2AK3, FOXP3, GATA4, GATA6, GCK, GLIS3, HNF1A, HNF1B, HNF4A, IER3IP1, INS, KCNJ11, KLF11, MNX1, NEUROD1, NEUROG3, NKX2-2, PAX4, PDX1, PPARG, PTF1A, RFX6, SLC19A2, WFS1, ZFP57

Monogenic Obesity Panel (68 genes) ADCY3, AFF4, ALMS1, ARL6, BBIP1, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BDNF, C8ORF37, CEP164, CEP19, CEP290, CPE, CREBBP, CUL4B, DYRK1B, EP300, FBN3, GNAS, GPR101, IFT172, IFT27, IFT74, KDM6A, KIDINS220, KIF7, KMT2D, KSR2, LEP, LEPR, LZTFL1, MAGEL2, MC3R, MC4R, MEGF8, MKKS, MKS1, MRAP2, NLGN2, NPY, NR0B2, NTRK2, PCSK1, PHF6, POMC, PPARG, PRMT7, RAB23, RAI1, RPS6KA3, SCLT1, SDCCAG8, SETD2, SH2B1, SIM1, TRAPPC3, TRAPPC9, TRIM32, TTC8, UCP3, VPS13B, WDPCP

Our cancer screening gives you a comprehensive genetic analysis on your risk of developing hereditary cancer.

Genes:
Multi-Cancer Panel (84 genes) AIP, ALK, APC, ATM, AXIN2, BAP1, BARD1, BLM, BMPR1A, BRCA1, BRCA2, BRIP1, CASR, CDC73, CDH1, CDK4, CDKN1B, CDKN1C, CDKN2A, CEBPA, CHEK2, CTNNA1, DICER1, DIS3L2, EGFR, EPCAM, FH, FLCN, GATA2, GPC3, GREM1, HOXB13, HRAS, KIT, MAX, MEN1, MET, MITF, MLH1, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NF2, NTHL1, PALB2, PDGFRA, PHOX2B, PMS2, POLD1, POLE, POT1, PRKAR1A, PTCH1, PTEN, RAD50, RAD51C, RAD51D, RB1, RECQL4, RET, RUNX1, SDHA, SDHAF2, SDHB, SDHC, SDHD, SMAD4, SMARCA4, SMARCB1, SMARCE1, STK11, SUFU, TERC, TERT, TMEM127, TP53, TSC1, TSC2, VHL, WRN, WT1

Common Hereditary Cancers Panel (47 genes) APC, ATM, AXIN2, BARD1, BMPR1A, BRCA1, BRCA2, BRIP1, CDH1, CDK4, CDKN2A, CHEK2, CTNNA1, DICER1, EPCAM, GREM1, HOXB13, KIT, MEN1, MLH1, MSH2, MSH3, MSH6, MUTYH, NBN, NF1, NTHL1, PALB2, PDGFRA, PMS2, POLD1, POLE, PTEN, RAD50, RAD51C, RAD51D, SDHA, SDHB, SDHC, SDHD, SMAD4, SMARCA4, STK11, TP53, TSC1, TSC2, VHL

Breast Cancer Guidelines-Based Panel (11 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, NF1, PALB2, PTEN, STK11, TP53

Oxy-Gen Breast Cancer Panel (26 genes) Primary Panel (13 genes) ATM, BARD1, BRCA1, BRCA2, CDH1, CHEK2, NF1, PALB2, PTEN, RAD51C, RAD51D, STK11, TP53
Add-on Preliminary-evidence Genes for Breast Cancer (13 genes) ABRAXAS1, AKT1, BRIP1, FANCC, FANCM, MRE11, MUTYH, PIK3CA, RECQL, RINT1, SDHB, SDHD, XRCC2

Breast and Gyn Cancers Guidelines-Based Panel (19 genes) ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, EPCAM, MLH1, MSH2, MSH6, NF1, PALB2, PMS2, PTEN, RAD51C, RAD51D, STK11, TP53

Breast and Gyn Cancers Panel (36 genes) Primary Panel (21 genes) ATM, BARD1, BRCA1, BRCA2, BRIP1, CDH1, CHEK2, DICER1, EPCAM, MLH1, MSH2, MSH6, NF1, PALB2, PMS2, PTEN, RAD51C, RAD51D, SMARCA4, STK11, TP53
Add-on Preliminary-evidence Genes for Breast and Gyn Cancer (15 genes) ABRAXAS1, AKT1, CDC73, FANCC, FANCM, MRE11, MUTYH, NBN, PIK3CA, POLD1, RECQL, RINT1, SDHB, SDHD, XRCC2

Colorectal Cancer Guidelines-Based Primary Panel (20 genes) APC, AXIN2, BMPR1A, CDH1, CHEK2, EPCAM, GREM1, MLH1, MSH2, MSH3, MSH6, MUTYH, NTHL1, PMS2, POLD1, POLE, PTEN, SMAD4, STK11, TP53
Add-on Preliminary-evidence Genes for Colorectal Cancer (10 genes) ATM, BLM, BUB1B, CEP57, ENG, FLCN, GALNT12, MLH3, RNF43, RPS20

Prostate Cancer Panel (19 genes) Primary Panel (12 genes) ATM, BRCA1, BRCA2, CHEK2, EPCAM, HOXB13, MLH1, MSH2, MSH6, NBN, PMS2, TP53
Add-on Preliminary-evidence Genes for Prostate Cancer (7 genes) ATR, BRIP1, FANCA, GEN1, PALB2, RAD51C, RAD51D

Nervous System/Brain Cancer Panel (42 genes) Primary Panel (29 genes) AIP, ALK, APC, DICER1, EPCAM, HRAS, LZTR1, MEN1, MLH1, MSH2, MSH6, NBN, NF1, NF2, PHOX2B, PMS2, POT1, PRKAR1A, PTCH1, PTEN, RB1, SMARCA4, SMARCB1, SMARCE1, SUFU, TP53, TSC1, TSC2, VHL
Add-on Preliminary-evidence Genes for Nervous System/Brain Cancer (5 genes) BAP1, EZH2, GPC3, KIF1B, PTCH2
Add-on Hereditary Paraganglioma-Pheochromocytoma Genes (8 genes) MAX, RET, SDHA, SDHAF2, SDHB, SDHC, SDHD, TMEM127

Melanoma Panel (12 genes) Primary Panel (9 genes) BAP1, BRCA2, CDK4, CDKN2A, MITF, POT1, PTEN, RB1, TP53
Add-on Preliminary-evidence Genes for Melanoma (3 genes) BRCA1, MC1R, TERT

Renal/Urinary Tract Cancers Panel (32 genes) Primary Panel (25 genes) BAP1, CDC73, CDKN1C, DICER1, DIS3L2, EPCAM, FH, FLCN, GPC3, MET, MLH1, MSH2, MSH6, PMS2, PTEN, REST, SDHB, SDHC, SMARCA4, SMARCB1, TP53, TSC1, TSC2, VHL, WT1
Add-on Preliminary-evidence Genes for Renal/Urinary Tract Cancers (7 genes) BUB1B, CEP57, CTR9, MITF, PALB2, SDHA, SDHD

Sarcoma Panel (44 genes) Primary Panel (29 genes) APC, BLM, CDKN1C, DICER1, EPCAM, EXT1, EXT2, FH, HRAS, KIT, MLH1, MSH2, MSH6, NBN, NF1, PDGFRA, PMS2, POT1, PRKAR1A, PTCH1, RB1, RECQL4, SDHA, SDHB, SDHC, SDHD, SUFU, TP53, WRN
Add-on Preliminary-evidence Genes for Sarcoma (4 genes) CDKN2A, PTCH2, TSC1, TSC2
Add-on Diamond-Blackfan Anemia Primary Genes (11 genes) GATA1, RPL11, RPL15, RPL26, RPL35A, RPL5, RPS10, RPS19, RPS24, RPS26, RPS7

Thyroid Cancer Panel (11 genes) Primary Panel (7 genes) APC, CHEK2, DICER1, PRKAR1A, PTEN, RET, TP53
Add-on Preliminary-evidence Genes for Thyroid Cancer (4 genes) MEN1, SDHB, SDHD, WRN

Prostate Cancer Panel 19 genes Primary Panel (12 genes) ATM, BRCA1, BRCA2, CHEK2, EPCAM, HOXB13, MLH1, MSH2, MSH6, NBN, PMS2, TP53
Add-on Preliminary-evidence Genes for Prostate Cancer (7 genes) ATR, BRIP1, FANCA, GEN1, PALB2, RAD51C, RAD51D

This screening is a medical examination designed to assess an individual’s risk for developing these neurological conditions.

Genes:
Hereditary Parkinson’s Disease and Parkinsonism (29 genes) Primary Panel (26 genes) ATP13A2, ATP7B, CHCHD2, CSF1R, DCTN1, DNAJC6, FBXO7, GBA, GCH1, LRRK2, PARK7, PDE8B, PINK1, PLA2G6, PRKN, PRKRA, RAB39B, SLC6A3, SNCA, SPR, SYNJ1, TH, TMEM230, VPS13C, VPS35, XPR1
Add-on Preliminary-evidence Genes for Hereditary Parkinson’s Disease and Parkinsonism (3 genes) MAPT, PODXL, UCHL1

Hereditary Amyotrophic Lateral Sclerosis, Frontotemporal Dementia, and Alzheimer’s Disease (43 genes) Primary Panel (34 genes) ALS2, ANG, ANXA11, APP, C9ORF72, CHCHD10, CHMP2B, DCTN1, ERBB4, FUS, GRN, HEXA, HNRNPA2B1, ITM2B, KIF5A, MAPT, OPTN, PFN1, PRNP, PSEN1, PSEN2, SETX, SNCA, SOD1, SORL1, SPG11, SQSTM1, TARDBP, TBK1, TFG, TREM2, UBQLN2, VAPB, VCP

Add-on Preliminary-evidence Genes for Hereditary Amyotrophic Lateral Sclerosis, Frontotemporal Dementia and Alzheimer Disease with C9orf72 (9 genes) ATP13A2, DDHD1, ERLIN1, FIG4, LRRK2, MATR3, NEFH, SIGMAR1, TIA1

Test over 554 genes to determine if you are a carrier of a genetic disorder that could be passed on to your children.

Genes:
Comprehensive Carrier Screen 569 genes Primary Panel (2 genes) CFTR, SMN1
Add-on Comprehensive Carrier Screen genes (554 genes) AAAS, ABCA12, ABCA3, ABCA4, ABCB11, ABCB4, ABCC2, ABCC8, ABCD1, ACAD9, ACADM, ACADVL, ACAT1, ACOX1, ACSF3, ADA, ADAMTS2, ADAMTSL4, ADGRG1, ADGRV1, AGA, AGL, AGPS, AGXT, AHI1, AIPL1, AIRE, ALDH3A2, ALDH7A1, ALDOB, ALG1, ALG13, ALG6, ALMS1, ALPL, AMN, AMT, ANO10, AP1S1, AQP2, AR, ARG1, ARL6, ARSA, ARSB, ARSE, ARX, ASL, ASNS, ASPA, ASS1, ATM, ATP6V1B1, ATP7A, ATP7B, ATP8B1, ATRX, AVPR2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BCKDHA, BCKDHB, BCS1L, BLM, BLOC1S3, BLOC1S6, BMP1, BRIP1, BSND, BTK, CAD, CANT1, CAPN3, CASQ2, CBS, CC2D1A, CC2D2A, CCDC103, CCDC39, CCDC88C, CD3D, CD3E, CD40, CD40LG, CD59, CDH23, CEP152, CEP290, CERKL, CHAT, CHM, CHRNE, CHRNG, CIITA, CLCN1, CLN3, CLN5, CLN6, CLN8, CLRN1, CNGB3, COL11A2, COL17A1, COL27A1, COL4A3, COL4A4, COL4A5, COL7A1, COX15, CPS1, CPT1A, CPT2, CRB1, CRTAP, CTNS, CTSA, CTSC, CTSD, CTSK, CYBA, CYBB, CYP11A1, CYP11B1, CYP11B2, CYP17A1, CYP19A1, CYP1B1, CYP21A2, CYP27A1, CYP27B1, CYP7B1, DBT, DCAF17, DCLRE1C, DDX11, DFNB59, DGAT1, DGUOK, DHCR7, DHDDS, DKC1, DLD, DLL3, DMD, DNAH11, DNAH5, DNAI1, DNAI2, DNMT3B, DOK7, DUOX2, DYNC2H1, DYSF, EDA, EIF2AK3, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, ELP1, EMD, EPG5, ERCC2, ERCC6, ERCC8, ESCO2, ETFA, ETFB, ETFDH, ETHE1, EVC, EVC2, EXOSC3, EYS, F9, FAH, FAM161A, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCG, FANCI, FANCL, FBP1, FBXO7, FH, FHL1, FKBP10, FKRP, FKTN, FMO3, FMR1, FOXN1, FOXRED1, FRAS1, FREM2, FUCA1, G6PC, G6PC3, GAA, GALC, GALE, GALK1, GALNS, GALNT3, GALT, GAMT, GATM, GBA, GBE1, GCDH, GCH1, GDF5, GFM1, GHR, GJB1, GJB2, GLA, GLB1, GLDC, GLE1, GNE, GNPAT, GNPTAB, GNPTG, GNS, GORAB, GRHPR, GRIP1, GSS, GUCY2D, GUSB, HADH, HADHA, HADHB, HAMP, HAX1, HBA1, HBA2, HBB, HCFC1, HEXA, HEXB, HGSNAT, HJV, HLCS, HMGCL, HMOX1, HOGA1, HPD, HPRT1, HPS1, HPS3, HPS4, HPS5, HPS6, HSD17B10, HSD17B3, HSD17B4, HSD3B2, HYAL1, HYLS1, IDS, IDUA, IGHMBP2, IKBKB, IL2RG, IL7R, INVS, ITGA6, ITGB3, ITGB4, IVD, JAK3, KCNJ1, KCNJ11, L1CAM, LAMA2, LAMA3, LAMB3, LAMC2, LARGE1, LCA5, LDLR, LDLRAP1, LHX3, LIFR, LIG4, LIPA, LMBRD1, LOXHD1, LPL, LRAT, LRP2, LRPPRC, LYST, MAK, MAN2B1, MANBA, MCEE, MCOLN1, MCPH1, MECP2, MECR, MED17, MESP2, MFSD8, MID1, MKKS, MKS1, MLC1, MLYCD, MMAA, MMAB, MMACHC, MMADHC, MOCS1, MOCS2, MPI, MPL, MPV17, MRE11, MTHFR, MTM1, MTR, MTRR, MTTP, MUSK, MUT, MVK, MYO15A, MYO7A, NAGA, NAGLU, NAGS, NBN, NCF2, NDRG1, NDUFAF2, NDUFAF5, NDUFS4, NDUFS6, NDUFS7, NDUFV1, NEB, NEU1, NGLY1, NPC1, NPC2, NPHP1, NPHS1, NPHS2, NR0B1, NR2E3, NSMCE3, NTRK1, OAT, OCA2, OCRL, OPA3, OSTM1, OTC, OTOA, OTOF, P3H1, PAH, PANK2, PC, PCBD1, PCCA, PCCB, PCDH15, PCNT, PDHA1, PDHB, PEPD, PET100, PEX1, PEX10, PEX12, PEX13, PEX16, PEX2, PEX26, PEX5, PEX6, PEX7, PFKM, PGM3, PHGDH, PHKB, PHKG2, PHYH, PIGN, PKHD1, PLA2G6, PLEKHG5, PLOD1, PLP1, PMM2, PNPO, POLG, POLH, POMGNT1, POMT1, POMT2, POR, POU1F1, PPT1, PRCD, PRDM5, PRF1, PROP1, PRPS1, PSAP, PTPRC, PTS, PUS1, PYGM, QDPR, RAB23, RAG1, RAG2, RAPSN, RARS2, RDH12, RLBP1, RMRP, RNASEH2A, RNASEH2B, RNASEH2C, RP2, RPE65, RPGRIP1L, RS1, RTEL1, RXYLT1, RYR1, SACS, SAMD9, SAMHD1, SCO2, SEC23B, SEPSECS, SGCA, SGCB, SGCD, SGCG, SGSH, SKIV2L, SLC12A1, SLC12A3, SLC12A6, SLC17A5, SLC19A2, SLC19A3, SLC1A4, SLC22A5, SLC25A13, SLC25A15, SLC25A20, SLC26A2, SLC26A3, SLC26A4, SLC27A4, SLC35A3, SLC37A4, SLC38A8, SLC39A4, SLC45A2, SLC4A11, SLC5A5, SLC6A8, SLC7A7, SMARCAL1, SMPD1, SNAP29, SPG11, SPR, SRD5A2, ST3GAL5, STAR, STX11, STXBP2, SUMF1, SUOX, SURF1, SYNE4, TANGO2, TAT, TAZ, TBCD, TBCE, TCIRG1, TCN2, TECPR2, TERT, TF, TFR2, TG, TGM1, TH, TK2, TMC1, TMEM216, TMEM67, TMPRSS3, TPO, TPP1, TREX1, TRIM32, TRIM37, TRMU, TSEN54, TSFM, TSHB, TSHR, TTC37, TTPA, TULP1, TYMP, TYR, TYRP1, UBR1, UNC13D, USH1C, USH2A, VDR, VLDLR, VPS11, VPS13A, VPS13B, VPS45, VPS53, VRK1, VSX2, WAS, WISP3, WNT10A, WRN, XPA, XPC, ZBTB24, ZFYVE26, ZNF469
Add-on genes with variable presentation (13 genes) BTD, F11, F2, F5, G6PD, GP1BA, GP9, HFE, HGD, MCCC1, MCCC2, MEFV, SERPINA1

Broad Carrier Screen 115 genes Primary Panel (2 genes) CFTR, SMN1
Add-on Broad Carrier Screen genes (113 genes) ABCA3, ABCC8, ABCD1, ACADM, ACADVL, ACAT1, AGA, AGXT, AHI1, AIRE, ALDOB, ALPL, ANO10, ARSA, ARX, ASL, ASPA, ASS1, ATP7B, BBS1, BBS2, BCKDHA, BCKDHB, BLM, CBS, CC2D2A, CCDC88C, CEP290, CHRNE, CLCN1, CLN3, CLRN1, CNGB3, COL7A1, CPT2, CYP11A1, CYP21A2, CYP27A1, CYP27B1, DHCR7, DHDDS, DLD, DMD, DYNC2H1, ELP1, ERCC2, EVC2, F9, FAH, FANCC, FKRP, FKTN, FMO3, FMR1, G6PC, GAA, GALC, GALT, GBA, GBE1, GJB2, GLA, GNPTAB, GRIP1, HBA1, HBA2, HBB, HEXA, HPS1, HPS3, IDUA, IL2RG, L1CAM, LRP2, MCOLN1, MCPH1, MID1, MLC1, MMACHC, MUT, MVK, NAGA, NEB, NPHS1, NPHS2, NR0B1, OCA2, OTC, PAH, PCDH15, PEX1, PEX6, PEX7, PKHD1, PLP1, PMM2, POLG, PRF1, RARS2, RNASEH2B, RS1, SCO2, SLC19A3, SLC26A2, SLC26A4, SLC37A4, SLC6A8, SMPD1, TF, TMEM216, TYR, USH2A, XPC

Core Carrier Screen 3 genes Primary Panel (2 genes) CFTR, SMN1
Add-on Core Carrier Screen genes (1 gene) FMR1

Broad Carrier Screen without X-linked Disorders 101 genes Primary Panel (2 genes) CFTR, SMN1
Add-on Broad Carrier Screen without X-linked Disorders genes (99 genes) ABCA3, ABCC8, ACADM, ACADVL, ACAT1, AGA, AGXT, AHI1, AIRE, ALDOB, ALPL, ANO10, ARSA, ASL, ASPA, ASS1, ATP7B, BBS1, BBS2, BCKDHA, BCKDHB, BLM, CBS, CC2D2A, CCDC88C, CEP290, CHRNE, CLCN1, CLN3, CLRN1, CNGB3, COL7A1, CPT2, CYP11A1, CYP21A2, CYP27A1, CYP27B1, DHCR7, DHDDS, DLD, DYNC2H1, ELP1, ERCC2, EVC2, FAH, FANCC, FKRP, FKTN, FMO3, G6PC, GAA, GALC, GALT, GBA, GBE1, GJB2, GNPTAB, GRIP1, HBA1, HBA2, HBB, HEXA, HPS1, HPS3, IDUA, LRP2, MCOLN1, MCPH1, MLC1, MMACHC, MUT, MVK, NAGA, NEB, NPHS1, NPHS2, OCA2, PAH, PCDH15, PEX1, PEX6, PEX7, PKHD1, PMM2, POLG, PRF1, RARS2, RNASEH2B, SCO2, SLC19A3, SLC26A2, SLC26A4, SLC37A4, SMPD1, TF, TMEM216, TYR, USH2A, XPC

Our immunodeficiency screening is a medical examination designed to assess if you have immune system issues.

Genes:
Primary Immunodeficiency Focus (108 genes) ADA, AICDA, ATM, B2M, BCL10, BLM, BLNK, BTK, CARD11, CCBE1, CD19, CD27, CD3D, CD3E, CD3G, CD40, CD40LG, CD79A, CD79B, CD81, CD8A, CHD7, CIITA, CR2, CTC1, CTLA4, DCLRE1C, DKC1, DNMT3B, DOCK8, EXTL3, FAT4, FOXN1, GATA2, ICOS, IGLL1, IKBKB, IL21R, IL2RG, IL7R, ITK, JAK3, KDM6A, KMT2D, LCK, LIG1, LRBA, LRRC8A, MAGT1, MALT1, MAP3K14, MCM4, MOGS, MS4A1, NBN, NFKB2, NFKBIA, NHEJ1, NHP2, NOP10, ORAI1, PIK3CD, PIK3R1, PLCG2, PNP, POLE, POLE2, RAG1, RAG2, RFX5, RFXANK, RFXAP, RHOH, RMRP, RNF168, RTEL1, SEMA3E, SH2D1A, SLC46A1, SMARCAL1, SP110, SPINK5, STAT3, STAT5B, STIM1, STK4, STXBP2, TBX1, TCF3, TCN2, TERC, TERT, TFRC, TINF2, TNFRSF13B, TNFRSF13C, TRNT1,TTC37, TTC7A, TYK2, UNG, USB1, WAS, WIPF1, WRAP53, XIAP, ZAP70, ZBTB24

Primary Immunodeficiency EXPANDED (146 genes) ADA, ADA2, ADAR, AICDA, AK2, ATM, B2M, BCL10, BLM, BLNK, BTK, CARD11, CCBE1, CD19, CD247, CD27, CD3D, CD3E, CD3G, CD40, CD40LG, CD79A, CD79B, CD81, CD8A, CHD7, CIITA, CORO1A, CR2, CTC1, CTLA4, CXCR4, DCLRE1C, DKC1, DNASE1L3, DNMT3B, DOCK8, ELANE, EXTL3, FAT4, FOXN1, G6PC, G6PC3, GATA2, HAX1, HPS1, HPS3, HPS4, HPS5, HPS6, ICOS, IFIH1, IGLL1, IKBKB, IL21R, IL2RG, IL7R, ITK, JAK3, KDM6A, KMT2D, LCK, LIG1, LIG4, LPIN2, LRBA, LRRC8A, MAGT1, MALT1, MAP3K14, MCM4, MEFV, MOGS, MS4A1, MTHFD1, MVK, NBN, NFKB2, NFKBIA, NHEJ1, NHP2, NLRC4, NLRP3, NOP10, ORAI1, PGM3, PIK3CD, PIK3R1, PLCG2, PNP, POLE, POLE2, PRKCD, PSTPIP1, PTPRC, RAC2, RAG1, RAG2, RFX5, RFXANK, RFXAP, RHOH, RMRP, RNASEH2A, RNASEH2B, RNASEH2C, RNF168, RTEL1, SAMHD1, SEMA3E, SH2D1A, SLC37A4, SLC46A1, SMARCAL1, SP110, SPINK5, STAT3, STAT5B, STIM1, STK4, STXBP2, TAZ, TBX1, TCF3, TCN2, TERC, TERT, TFRC, TINF2, TNFRSF13B, TNFRSF13C, TNFRSF1A, TREX1, TRNT1, TTC37, TTC7A, TYK2, UNG, USB1, VPS13B, WAS, WIPF1, WRAP53, XIAP, ZAP70, ZBTB24

Primary Immunodeficiency Plus (19 genes) BLM, BRCA2, CFTR, F5, F9, FANCC, G6PC, G6PD, JAK2, MPL, MSH6, MYD88, NRAS, PALB2, PLCG2, PMS2, PTEN, RUNX1, TERT

Test 186 genes to assess your risk of developing an inherited form of cardiovascular (heart) disease.

Genes:
Hereditary Cardio Screen (117 genes) ABCC9, ACTA2, ACTC1, ACTN2, ACVRL1, AGL, AKAP9, ALMS1, ANK2, APOB, BAG3, BMPR2, CACNA1C, CACNA1S, CACNB2, CALM1, CALM2, CALM3, CASQ2, CAV1, CAV3, COL3A1,CRYAB, CSRP3,DES,DMD,DOLK,DSC2,DSG2,DSP,EMD,ENG,EYA4,F9,FBN1,FHL1,FKRP,FKTN,FLNC,GAA,GATAD1,GDF2,GLA,GPD1L,HCN4,JPH2,JUP, KCNA5, KCND3, KCNE1, KCNE2, KCNE3, KCNH2, KCNJ2, KCNJ5, KCNQ1, LAMA4, LAMP2, LDB3, LDLR, LDLRAP1, LMNA, MYBPC3, MYH11, MYH6, MYH7, MYL2, MYL3, MYLK, MYOZ2, MYPN, NEXN, NKX2-5, PCSK9, PKP2, PLN, PRKAG2, PRKG1, PROC, PROS1, PTPN11, RAF1, RBM20, RIT1, RYR1, RYR2, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SCN5A, SERPINC1, SGCD, SLC22A5, SMAD3, SMAD4, SNTA1, SOS1, TAZ, TBX20, TBX5, TCAP, TGFB2, TGFB3, TGFBR1, TGFBR2, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TRDN, TRPM4, TTN, TTR, VCL

Hereditary Cardio Screen Focus (44 genes) ACTA2, ACTC1, APOB, BAG3, CACNA1S, COL3A1, DES, DSC2, DSG2, DSP, F9, FBN1, FLNC, GLA, JUP, KCNH2, KCNQ1, LDLR, LMNA, MYBPC3, MYH11, MYH7, MYL2, MYL3, MYLK, PCSK9, PKP2, PRKAG2, PRKG1, RBM20, RYR1, RYR2, SCN5A, SMAD3, TGFB2, TGFBR1, TGFBR2, TMEM43, TNNC1, TNNI3, TNNT2, TPM1, TTN, TTR

Actionable Cardiovascular (32 genes) ACTA2,ACTC1,APOB,CACNA1S,COL3A1,DSC2,DSG2,DSP, FBN1,GLA,KCNH2,KCNQ1,LDLR,LMNA,MYBPC3,MYH11,MYH7,MYL2,MYL3,PCSK9,PKP2,PRKAG2,RYR1, RYR2, SCN5A, SMAD3, TGFBR1, TGFBR2, TMEM43, TNNI3, TNNT2, TPM1

Long QT Syndrome Panel 17 genes Primary Panel (10 genes) CACNA1C, CALM1, CALM2, CALM3, KCNE1, KCNH2, KCNJ2, KCNQ1, SCN5A, TRDN
Add-on Preliminary-evidence Genes for Long QT Syndrome (7 genes) AKAP9, ANK2, CAV3, KCNE2, KCNJ5, SCN4B, SNTA1

Familial Hypercholesterolemia (4 genes) APOB, LDLR, LDLRAP1, PCSK9

Arrhythmia and Cardiomyopathy Comprehensive Panel 186 genes Primary Panel (100 genes) ABCC9, ACADVL, ACTC1, ACTN2, AGL, ALMS1, ALPK3, BAG3, BRAF, CACNA1C, CACNA1D, CALM1, CALM2, CALM3, CASQ2, CBL, CDH2, CPT2, CRYAB, CSRP3, DES, DMD, DNAJC19, DOLK, DSC2, DSG2, DSP, ELAC2, EMD, EYA4, FHL1, FKRP, FKTN, FLNC, GAA, GATA4, GATA5, GJA5, GLA, HCN4, HRAS, JUP, KCNE1, KCNH2, KCNJ2, KCNQ1, KRAS, LAMP2, LMNA, LZTR1, MAP2K1, MAP2K2, MRAS, MTO1, MYBPC3, MYH7, MYL2, MYL3, MYL4, MYLK3, NF1, NKX2-5, NRAS, PCCA, PCCB, PKP2, PLN, PPA2, PPCS, PPP1CB, PRKAG2, PTPN11, RAF1, RASA1, RBM20, RIT1, RYR2, SCN5A, SDHA, SGCD, SHOC2, SLC22A5, SOS1, SOS2, SPRED1, TAZ, TBX20, TCAP, TMEM43, TMEM70, TNNC1, TNNI3, TNNI3K, TNNT2, TPM1, TRDN, TRPM4, TTN, TTR, VCL
Add-on Preliminary-evidence Genes for Arrhythmia and Cardiomyopathy (57 genes) A2ML1, AKAP9, ANK2, ANKRD1, CACNA2D1, CACNB2, CALR3, CAV3, CHRM2, CTF1, CTNNA3, DTNA, FHL2, GATA6, GATAD1, GPD1L, HAND1, ILK, JPH2, KCNA5, KCND3, KCNE2, KCNE3, KCNE5, KCNJ5, KCNJ8, KCNK3, KIF20A, KLF10, LAMA4, LDB3, LRRC10, MAP3K8, MED12, MYH6, MYLK2, MYOM1, MYOZ2, MYPN, NEBL, NEXN, NPPA, PDLIM3, PLEKHM2, PRDM16, RANGRF, RASA2, RRAS, SCN10A, SCN1B, SCN2B, SCN3B, SCN4B, SLMAP, SNTA1, TMPO, TXNRD2
Add-on Sudden Unexpected Death in Epilepsy (SUDEP) Genes (11 genes) DEPDC5, KCNA1, KCNQ2, KCNQ3, KCNT1, PCDH19, PRRT2, SCN1A, SCN8A, SCN9A, SLC2A1

Test specific genes to assess how your genes impact your response to current medications you’re taking.

Genes:
Mental Health Panel: CYP2C19, CYP2D6, CYP3A4, CYP3A5

Psych Panel: CYP2C19, CYP2D6, CYP3A4, CYP3A5, COMPT, MTHFR

Focus Panel: BCHE, CYP2B6, CYP2C19, CYP2C9, CYP2D6, CYP3A5, CYP4F2, DPYD, G6PD, HLA-B, IFNL4, NAT2, NUDT15, RYR1, SLCO1B1, TPMT, UGT1A1, VKORC1

Cardio Panel: APOE, CYP2C9, CYP2C9, CYP2C19, CYP2D6, CYP3A4, CYP3A5, Factor II, Factor V Leiden, MTHFR, SLCO1B1, VKORC1