Testing for >900 conditions using your DNA

Why Genetics?

Understand your inherited health risks and make confident decisions with expert support from Jeen.

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How it works

Chat with our Genetic Counsellor, receive your at-home DNA kit with a quick cheek swab, send it back, and get your results in under 4 weeks.

Why Genetics Matters?

Your DNA holds valuable clues about your health. Genetic testing helps you discover inherited risks—like certain cancers or conditions you could pass to your children. At Jeen Health, we make this science simple, accessible, and personal.

With expert-led guidance and an easy at-home test, you can take control of your health journey. Whether you're planning a family, concerned about cancer, or just want answers—genetic testing offers clarity and confidence.

Metabolic Disorders
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Associated Genes:
AAAS, ABCB11, ABCB4, ABCD1, ABCD4, ACAD9, ACADM, ACADS, ACADSB, ACADVL, ACAT1, ACOX1, ACSF3, ADA, ADSL, AGPS, AGXT, AHCY, ALAD, ALDH3A2, ALDH4A1, ALDH7A1, ALDOB, ALG1, ALG12, ALG3, ALG6, ALOX12B, ALPL, AMT, ARSA, ARSB, ARSE, ASL, ASNS, ASPA, ASS1, AUH, BCKDHA, BCKDHB, BTD, CBS, CETP, CFTR, CLCN5, CPS1, CPT1A, CPT2, CYP11A1, CYP11B1, CYP11B2, CYP17A1, CYP21A2, CYP27A1, CYP27B1, DBT, DHCR24, DHCR7, DLAT, DLD, DPYD, ETFA, ETFB, ETFDH, FAH, FBP1, FOLR1, FTCD, G6PC, G6PC3, G6PD, GAA, GALE, GALK1, GALNS, GALT, GAMT, GATM, GBA, GBE1, GCDH, GLA, GLB1, GLDC, GLUD1, GNMT, GRHPR, GSS, GUSB, GYS2, HADH, HADHA, HADHB, HCFC1, HEXA, HEXB, HLCS, HMGCL, HMGCS2, HOGA1, HPD, HSD17B10, HSD17B3, HSD17B4, HSD3B2, HSD3B7, HYAL1, IDS, IDUA, IVD, LIPA, MAT1A, MCCC1, MCCC2, MCEE, MCOLN1, MLYCD, MMAA, MMAB, MMACHC, MMADHC, MPI, MTHFR, MTR, MTRR, MUT, NAGS, NEU1, NGLY1, NPC1, NPC2, OAT, OTC, PAH, PC, PCBD1, PCCA, PCCB, PDHA1, PDHB, PDHX, PDP1, PEPD, PFKM, PGAM2, PGK1, PHEX, PHGDH, PHKA1, PHKA2, PHKB, PHKG2, PHYH, PKD1, PKD2, PKHD1, PLA2G6, PMM2, PNP, PNPO, POLG, POMGNT1, POMT1, POMT2, POR, PPOX, PPT1, PRKAG2, PSAP, PTS, PYGL, PYGM, QDPR, RSPH9, SGSH, SLC12A1, SLC12A3, SLC17A5, SLC19A2, SLC19A3, SLC22A5, SLC25A13, SLC25A15, SLC25A20, SLC26A2, SLC26A3, SLC2A1, SLC2A2, SLC35A3, SLC37A4, SLC3A1, SLC5A5, SLC6A19, SLC6A8, SLC7A7, SLC7A9, SMPD1, SPR, STAR, SUMF1, TAT, TPP1, TTPA, TYR, TYMP, UGT1A1
Associated Conditions:
Includes phenylketonuria (PKU), galactosemia, Tay-Sachs disease, Gaucher disease, glycogen storage diseases, maple syrup urine disease, organic acidemias, fatty acid oxidation disorders, urea cycle disorders, lysosomal storage disorders, peroxisomal disorders, and other inborn errors of metabolism
Blood Disorders
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Associated Genes:
ANK1, CYBA, CYBB, EPB42, F2, F5, F7, F8, F9, F11, FERMT3, G6PD, GP1BA, GP9, HBA1, HBA2, HBB, HFE, HAMP, HJV, ITGA2B, ITGB3, MPL, NBN, NCF2, NCF4, PIGA, PKLR, RHAG, SEC23B, SLC4A1, SPTA1, SPTB, TF, TFR2, TPI1, VWF, WAS
Associated Conditions:
Hemoglobinopathies (sickle cell anemia, beta thalassemia, alpha thalassemia), G6PD deficiency, hemophilia, hereditary spherocytosis, clotting disorders, Fanconi anemia, and other hematological conditions
Neuromuscular Disorders
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Associated Genes:
CAPN3, CHAT, CHRNE, CHRNG, CLCN1, COLQ, DMD, DYSF, FKRP, FKTN, MTM1, NEB, PLEC, POMGNT1, POMT1, POMT2, SGCA, SGCB, SGCD, SGCG, SLC5A7, SMN1, TTN
Associated Conditions:
Muscular dystrophies (Duchenne, Becker, limb-girdle, congenital), spinal muscular atrophy, myasthenic syndromes, and other disorders affecting skeletal muscles and neuromuscular junctions
Sensory Disorders
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Associated Genes:
ADGRV1, AIPL1, CACNA1F, CABP2, CDH23, CERKL, CHM, CHST6, CIB2, CLRN1, CNGA1, CNGA3, CNGB1, CNGB3, CRB1, CYP4V2, DFNB31, ELOVL4, EYS, FRMD7, GDF6, GJB2, GJB6, GPR143, GRM6, GUCY2D, KCNJ13, KCNV2, LCA5, LHON, LOXHD1, LRAT, MAK, MERTK, MITF, MYO7A, NDP, NR2E3, NYX, OCA2, OTOF, PAX2, PAX6, PCDH15, PDE6A, PDE6B, PDZD7, PROM1, PRPF31, PRPF8, RB1, RD3, RDH12, RDH5, RLBP1, RP1, RP2, RPE65, RPGR, RPGRIP1, RS1, SAG, SLC24A1, SLC26A4, SNRNP200, STRC, TCOF1, TECTA, TMC1, TMEM67, TMPRSS3, TYR, USH1C, USH1G, USH2A, WHRN
Associated Conditions:
Hereditary hearing loss (connexin-related and other forms), Usher syndrome, retinitis pigmentosa, Leber congenital amaurosis, albinism, and other disorders affecting vision, hearing, or both
Neurological Disorders
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Associated Genes:
ABCD1, AFF2, AIMP1, ALS2, AP1S2, APP, ARSA, ARX, ASPA, ATM, ATP13A2, ATP1A3, ATP6AP2, ATP7A, ATP7B, ATRX, BRWD3, CACNA1A, CDKL5, CLN3, CLN5, CLN6, CLN8, CNTNAP2, CSTB, CTC1, CTSD, CTSF, CUL4B, DCX, DKC1, DLG3, DNMT3B, DYNC1H1, ELOVL4, EMX2, FAM126A, FGD1, FMR1, FOXG1, FOXP1, FTSJ1, FXN, GCH1, GJC2, GLRA1, HEXA, HEXB, IGHMBP2, IKBKAP, JAG1, KCNA1, KCNQ2, KCNQ3, KDM5C, KIAA0196, L1CAM, LAMA2, LARGE1, LMNB1, MBD5, MECP2, MLC1, NAGLU, NFIX, NIPA1, NLGN3, NLGN4X, NONO, NOTCH3, NRXN1, NTRK1, OPHN1, PAFAH1B1, PAK3, PARK2, PARK7, PDHA1, PHF6, PHF8, PINK1, PLA2G6, PLP1, POLG, POMGNT1, POMT1, POMT2, PPT1, PQBP1, PRPS1, PRRT2, PTCH1, PTCHD1, PTEN, PTPN11, RAB39B, RAI1, RELN, ROGDI, RTN2, SACS, SATB2, SCN1A, SCN1B, SCN2A, SCN8A, SERPINI1, SHANK2, SHANK3, SLC16A2, SLC1A3, SLC2A1, SLC6A8, SLC9A6, SMARCB1, SMPD1, SNRPN, SOX10, SPAST, SPG11, SPG7, STXBP1, SYN1, SYNGAP1, TBR1, TCF4, THOC2, TRAPPC9, TSC1, TSC2, TTR, UBE3A, UPF3B, VLDLR, VPS13A, XPA, ZEB2, ZFHX1B, ZDHHC9, ZNF41, ZNF674, ZNF711, ZNF81
Associated Conditions:
Fragile X syndrome, leukodystrophies, Canavan disease, spastic paraplegias, ataxias, adrenoleukodystrophy, Rett syndrome, Wilson disease, spinocerebellar ataxias, neuronal ceroid lipofuscinoses, and other disorders affecting the central and peripheral nervous systems
Connective Tissue & Skeletal Disorders
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Associated Genes:
ADAMTS2, ADAMTSL2, ALMS1, ALX4, ANTXR2, BMP1, BMPER, BMPR1A, CENPJ, CEP152, CEP290, CEP63, CHST14, COL11A1, COL11A2, COL17A1, COL18A1, COL1A1, COL1A2, COL27A1, COL2A1, COL3A1, COL4A3, COL4A4, COL4A5, COL5A1, COL5A2, COL6A1, COL6A2, COL7A1, COL9A1, COL9A2, COMP, CRTAP, CUL7, DDR2, DLL3, DNAJC21, DPYD, DTDST, DYNC2H1, EBP, EFNB1, EFTUD2, ELN, ERCC6, EVC, EVC2, FAM20C, FBN1, FBN2, FGFR1, FGFR2, FGFR3, FLNA, FLNB, FOXC1, FOXC2, GDF5, GJA1, GLI3, GNAS, GNPTAB, GNPTG, GNRHR, HDAC8, HES7, IFT80, IHH, IKBKG, LFNG, LMNA, LRP5, MASP1, MATN3, MEGF8, MESP2, MMP2, MMP9, MMP13, MSX1, MSX2, MYH3, NIPBL, NKX3-2, NOG, NOTCH1, P3H1, PAX3, PCNT, PEX7, PLOD1, PLOD2, PLOD3, POLR1A, POLR1C, POLR1D, POLR3A, POLR3B, POR, PRDM5, PTCH1, PTCH2, PYCR1, RAD21, RECQL4, ROR2, RUNX2, SBDS, SCARF2, SERPINF1, SHH, SHOX, SIX3, SLC26A2, SLC35D1, SMC1A, SMC3, SOX9, TBCE, TCOF1, TGFBR1, TGFBR2, TNFRSF11A, TNFRSF11B, TNXB, TP63, TRPS1, TWIST1, WISP3, WNT1, WNT10A, ZIC2, ZNF469
Associated Conditions:
Osteogenesis imperfecta, Ehlers-Danlos syndromes, Marfan syndrome, Stickler syndrome, chondrodysplasias, Alport syndrome, epidermolysis bullosa, craniosynostosis syndromes, and other disorders affecting connective tissue, bones, and cartilage
Primary Immunodeficiencies
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Associated Genes:
ADA, AIRE, AK2, BTK, CD3D, CD3E, CD3G, CD40LG, CD79A, CD79B, CD8A, CIITA, CORO1A, CTLA4, CYBA, CYBB, DCLRE1C, DOCK8, FOXN1, FOXP3, GATA2, ICOS, IKBKB, IL10, IL10RA, IL10RB, IL12B, IL12RB1, IL17F, IL17RA, IL1RN, IL21, IL21R, IL2RA, IL2RG, IL7R, ITK, JAK3, LRBA, LYST, MALT1, MVK, NCF2, NCF4, NLRP3, ORAI1, PIK3CD, PIK3R1, PNP, PRF1, PRKDC, PTPRC, RAG1, RAG2, RBCK1, RFX5, RFXANK, RFXAP, SH2D1A, SP110, STAT1, STAT3, STAT5B, STX11, STXBP2, TAP1, TAP2, TAPBP, TERT, TINF2, TNFRSF13B, TNFRSF13C, TNFRSF1A, TTC7A, UNC13D, WAS, WRAP53, XIAP, ZAP70
Associated Conditions:
Severe combined immunodeficiency (SCID), X-linked agammaglobulinemia, chronic granulomatous disease, Wiskott-Aldrich syndrome, hyper-IgM syndrome, hyper-IgE syndrome, common variable immunodeficiency, and other disorders affecting immune system development and function
Kidney & Urinary Tract Disorders
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Associated Genes:
ACE, AGTR1, AQP2, ATP6V0A4, ATP6V1B1, AVPR2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, CLCN5, CLCNKB, COL4A3, COL4A4, COL4A5, CTNS, CYP24A1, GRHPR, HNF1B, HOGA1, KCNJ1, MKKS, NPHP1, NPHP3, NPHS1, NPHS2, OCRL, PKHD1, SLC12A1, SLC12A3, SLC22A12, SLC2A9, SLC34A1, SLC34A3, SLC3A1, SLC4A1, SLC7A9, SLC9A3R1, UMOD, VDR, WDR19, WT1
Associated Conditions:
Polycystic kidney disease, Alport syndrome, nephrotic syndrome, cystinosis, Bartter syndrome, Gitelman syndrome, renal tubular acidosis, nephronophthisis, and other disorders affecting kidney structure and function
Endocrine Disorders
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Associated Genes:
ABCC8, AMH, AMHR2, AR, AVP, CASR, CYP11A1, CYP11B1, CYP11B2, CYP17A1, CYP19A1, CYP21A2, DIO2, DUOX2, DUOXA2, GH1, GHR, GHRHR, GNAS, GNRH1, GNRHR, HESX1, HSD17B3, HSD3B2, IGSF1, IYD, KCNJ11, KISS1, KISS1R, LHB, LHCGR, LHX3, LHX4, MC2R, MC4R, MKRN3, NKX2-1, NR0B1, NR5A1, POU1F1, POMC, PRDM16, PROP1, SHH, SLC16A2, SOD2, SOX2, SOX3, STAR, TBX19, THRA, THRB, TG, THRA, TPO, TRHR, TSHB, TSHR, VDR
Associated Conditions:
Congenital adrenal hyperplasia, disorders of sex development, congenital hypothyroidism, growth hormone deficiency, diabetes, hypogonadotropic hypogonadism, and other disorders affecting the endocrine glands and hormone production
Other Genetic Disorders
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Associated Genes:
All remaining genes not categorized above: ADGRG1, ALOX12B, ALOXE3, AP1S1, AP3B1, AP3D1, AP4E1, AP4M1, AP4S1, APOPT1, ARL13B, ARL6, B9D1, B9D2, BLOC1S3, BLOC1S6, BRAF, BRIP1, CAVIN1, CC2D1A, CC2D2A, CCDC103, CCDC151, CCDC39, CCDC8, CCDC88C, CD247, CDK13, CDKN1C, CDSN, CERS3, CFAP53, CILK1, CLP1, CPLANE1, CRADD, CWC27, DCAF17, DGUOK, DHPS, DKC1, DLL1, DNM1L, DYNC2H1, EMD, EP300, EXOSC3, FA2H, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, FBXL4, FERMT1, FH, FHL1, FKBP10, FLVCR1, GFM1, GJB1, GLE1, GNAI3, GORAB, GRIP1, HACE1, HPS1, HPS3, HPS4, HPS5, HPS6, HYLS1, INPP5E, INVS, KAT6B, KIF14, KIF7, KMT2A, KMT2D, LARP7, LARS, LEMD3, LIFR, LIG4, LIPA, LIPN, LMAN1, LMBRD1, LPAR6, MED17, MEFV, MITF, MMUT, MYO15A, NAGA, NAGLU, NBAS, NBEAL2, NIN, NHEJ1, NIPAL4, NOD2, NOP10, NRAS, OSTM1, P4HB, PAX8, PEX13, PGAP3, PLCE1, PLEKHM1, PMM2, POMC, PTCH1, PTCH2, PYCR1, RECQL3, RMRP, RNASEH2A, RNASEH2B, RNASEH2C, RNU4ATAC, RP1L1, RPGRIP1L, RTEL1, SARS2, SBDS, SCARF2, SCO1, SCO2, SDR9C7, SDCCAG8, SEC23B, SELENON, SEPSECS, SERPINF1, SF3B4, SGMS2, SH3TC2, SIX5, SKIV2L, SLC24A5, SLC26A4, SLC27A4, SLC2A10, SLC39A4, SLC45A2, SLC46A1, SLURP1, SMAD4, SMARCAL1, SNAI2, SNRNP200, SNX10, SOX10, SPG7, SPINK5, ST3GAL5, SUOX, SURF1, TAF1, TAZ, TBCE, TBXAS1, TCIRG1, TCTN1, TCTN2, TCTN3, TECPR2, TERC, TERT, TFAP2A, TGIF1, TIMM8A, TINF2, TMEM107, TMEM138, TMEM216, TMEM231, TMEM237, TMEM38B, TMEM67, TMEM70, TNF, TNXB, TRAF7, TRAPPC11, TRDN, TRIM37, TRMU, TRPM6, TSEN2, TSEN34, TSEN54, TSFM, TTC21B, TTC37, TTC8, TUBB1, TUBB3, TUBGCP4, TUBGCP6, TULP1, TYRP1, USP9X, VPS13B, VPS33B, VPS45, VPS53, VRK1, VSX2, WDR19, WDR34, WDR35, WDR60, WISP3, WRAP53, WRN, YAP1, ZAP70, ZBTB24, ZFYVE26, ZIC1, ZIC2
Associated Conditions:
Various other genetic conditions including ciliopathies, developmental disorders, mitochondrial disorders, DNA repair disorders, and rare syndromes that do not fit neatly into the categories above
Total genes in panel: 787