Testing for >1000 conditions using your DNA

Why Genetics?

Know your inherited risks. Get expert support and reliable genetic testing in UK with 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.

Gene List

Learn about our carefully selected list of
genes relating to carrier risk

Metabolic Disorders
+
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
+
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
+
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
+
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
+
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
+
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
+
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
+
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
+
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
+
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

Type of Cancers

Type of Cancers

We offer expert advice and testing for a range of genes that may increase your risk of developing certain types of cancer.

View Full Gene List

Another 23 & Me?

At Jeen, we focus on health, not hair colour. Our genetic testing uses 50x sequencing depth for greater accuracy and confidence in detecting inherited conditions.

Genetic
Counselling

What do we test for?

Know your genes, protect your future. Over 5,000 diseases are linked to genetic mutations. Early insights through genetic testing can help with prevention, early detection and personalised healthcare decisions.

Other Genetic Conditions

Over 5,000 diseases are linked to genetic mutations

Coming Soon
Hereditary Cancer Risk

Testing 154 Genes Linked With Various Cancers

Learn More
Other Genetic Conditions

Over 5,000 diseases are linked to genetic mutations

Coming Soon

Frequently
Asked Questions

What is genetic testing?

Genetic testing looks at your DNA to find changes or variants in your genes. These changes can tell us if you’re at risk for certain inherited conditions, like hereditary cancers or if you’re a carrier for a genetic condition.

What can genetic testing tell me?

It can reveal if you have a higher genetic risk for certain cancers (like breast, ovarian or bowel), if you’re a carrier for inherited conditions, or if you have a genetic condition that could impact your health or your family’s.

Will the results tell me if I’ll definitely get a disease?

No - genetic testing shows your risk, not a guarantee. Some people with a genetic variant never develop the condition, while others without a variant might still be affected due to lifestyle or environmental factors.

How does it work?

It’s simple - you speak with one of our expert Genetic Counsellors, receive a home kit in the post, collect a cheek swab, and send it back. Your DNA is analysed in a UK or US lab, and results are ready in under 4 weeks.

Is my data safe and private?

Yes. At Jeen Health, your data is encrypted and stored securely on our GDPR compliant servers, as well as with our vetted laboratories. Your results are only shared with you and your dedicated Genetic Counsellor, never with insurers or third parties.

Is genetic testing only for people with a family history of disease?

Not at all. While a strong family history increases your risk, many people with genetic conditions have no known family history. Testing helps you uncover hidden risks you wouldn’t otherwise know about.

Get in touch

Our team of expert Genetic Counsellors is here to help. Whether you're curious about testing, your results, or what’s right for you — we're just a message away.

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