Testing for >1000 conditions using your DNA

Why Genetics?

Know your and your family's genetic risks. Get expert support and reliable genetic testing in UK with Jeen.

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Speak to a Genetic Counsellor Today

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.

How it works

Trusted specialists

Spital Clinic - Top rated Primary Care Clinic in London on Doctify
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.

1

Online Specialist Counselling

Speak to our expert geneticists/midwifes,
design your personalised test

2

Bloods Test

Get your test through the mail,
easy oral self-swab

3

Report & Recommendations

Get your detailed report and
recommendations

Gene List

Gene Category Associated Genes Conditions
Metabolic Disorders AAAS, ABCA12, ABCA3, ABCA4, ABCB11, ABCB4, ABCC8, ABCD1, ABCD4, ACAD9, ACADM, ACADS, ACADSB, ACADVL, ACAT1, ACOX1, ACSF3, ADA, AGA, AGL, AGPAT2, AGPS, AGXT, AHCY, AKR1D1, ALDH3A2, ALDH4A1, ALDH7A1, ALDOB, ALG1, ALG12, ALG3, ALG6, ALOX12B, ALOXE3, ALPL, AMN, AMT, ANTXR2, ARG1, ARSA, ARSB, ARSE, ASL, ASNS, ASPA, ASS1, ATM, ATP7A, ATP7B, ATP8B1, BCHE, BCKDHA, BCKDHB, BCS1L, BTD, CANT1, CBS, COQ4, COX10, COX15, COX20, COX6B1, CP, CPS1, CPT1A, CPT2, CRADD, CTNS, CTSA, CTSC, CTSD, CTSF, CTSK, CYBA, CYBB, DBT, DDC, DGUOK, DHCR24, DHCR7, DHDDS, DLAT, DLD, DPYD, ETFA, ETFB, ETFDH, ETHE1, FA2H, FAH, FBXL4, FBP1, FH, FMO3, FOLR1, FOXRED1, FTCD, FUCA1, FXN, G6PC, G6PC3, G6PD, GAA, GALC, GALE, GALK1, GALNS, GALNT3, GALT, GAMT, GATM, GBA, GBE1, GCDH, GDAP1, GFPT1, GLA, GLB1, GLDC, GNE, GNS, GRHPR, GSS, GUSB, GYS2, HADH, HADHA, HADHB, HAX1, HCFC1, HEXA, HEXB, HGD, HGSNAT, HINT1, HLCS, HMGCL, HMGCS2, HOGA1, HPD, HPS1, HPS3, HPS4, HPS5, HPS6, HSD17B10, HSD17B3, HSD17B4, HSD3B2, HSD3B7, HYAL1, IDH3B, IDS, IDUA, ITPA, IVD, LIPA, LIPN, MAT1A, MCCC1, MCCC2, MCEE, MCOLN1, MLYCD, MMAA, MMAB, MMACHC, MMADHC, MPI, MPV17, MTHFD1, MTHFR, MTR, MTRR, MTTP, MUT, MVK, NAGA, NAGLU, NAGS, NEU1, NGLY1, NPC1, NPC2, OAT, OTC, PAH, PANK2, PC, PCBD1, PCCA, PCCB, PDHA1, PDHB, PDHX, PDP1, PEPD, PET100, PFKM, PGK1, PHGDH, PHKA1, PHKA2, PHKB, PHKG2, PHYH, PMM2, PNP, PNPO, PPT1, PRPS1, PSAP, PTS, PYGL, PYGM, QDPR, RTEL1, SACS, SAMD9, SAMHD1, SARS2, SBDS, SCO1, SCO2, SERPINA1, SGSH, SLC12A1, SLC12A3, SLC16A2, SLC17A5, SLC19A2, SLC19A3, SLC22A5, SLC25A13, SLC25A15, SLC25A20, SLC26A2, SLC26A3, SLC27A4, SLC34A3, SLC35A3, SLC37A4, SLC39A4, SLC3A1, SLC45A2, SLC46A1, SLC4A1, SLC5A5, SLC6A19, SLC6A8, SLC7A7, SLC7A9, SMPD1, SPR, SUCLA2, SUMF1, SUOX, SURF1, TAT, TERT, TF, TFR2, TG, TGM1, TH, TK2, TPP1, TTPA, TYMP, TYR, TYRP1, UGT1A1 Inborn errors of metabolism including amino acid disorders (PKU, maple syrup urine disease), organic acidemias, fatty acid oxidation disorders, urea cycle disorders, glycogen storage diseases, lysosomal storage disorders, peroxisomal disorders, porphyria, and other metabolic conditions
Blood & Coagulation Disorders EPB42, F11, F2, F5, F7, F8, F9, GP1BA, GP9, HAMP, HBA1, HBA2, HBB, HFE, HJV, ITGA2B, ITGA6, ITGB3, ITGB4, MPL, NBEAL2, NBN, NCF2, NCF4, RHAG, SEC23B, CDAN1, PGM3 Hemoglobinopathies (sickle cell disease, thalassemias), bleeding disorders (hemophilia, von Willebrand disease), platelet disorders, iron metabolism disorders, and other hematological conditions
Neuromuscular Disorders CAPN3, CASP14, CHAT, CHRNE, CHRNG, CLCN1, COLQ, DMD, DOK7, DYSF, FKBP10, FKRP, FKTN, FHL1, MTM1, MTMR2, NEB, PLEKHG5, POMGNT1, POMT1, POMT2, RAPSN, SELENON, SGCA, SGCB, SGCD, SGCG, SLC5A7, SMN1, TAZ, ESCO2 Muscular dystrophies (Duchenne, Becker, limb-girdle), congenital myopathies, spinal muscular atrophy, myasthenic syndromes, and neuromuscular junction disorders
Sensory Disorders (Hearing & Vision) ABCA4, AIPL1, CDH23, CERKL, CHM, CHST6, CIB2, CLRN1, CNGA1, CNGA3, CNGB1, CNGB3, CRYL1, EYS, FAM161A, GJB1, GJB2, GJB6, GPR143, GUCY2D, LHCGR, LOXHD1, LRAT, MAK, MYO7A, NDP, NR2E3, OCA2, OPA3, OTOF, PCDH15, PDE6A, PJVK, PRCD, PRDM5, RD3, RDH12, RDH5, RLBP1, RP2, RPE65, RPGR, RPGRIP1, RPGRIP1L, RS1, SAG, TMPRSS3, USH1C, USH1G, USH2A, WHRN, SLC26A4, CRB1 Hereditary hearing loss (non-syndromic and syndromic), Usher syndrome, retinitis pigmentosa, Leber congenital amaurosis, albinism, color blindness, and other vision/hearing disorders
Neurological & Neurodevelopmental Disorders ADGRG1, ADGRV1, AFF2, AHI1, AIMP1, AIRE, ARX, ATRX, BLM, BRWD3, CC2D1A, CC2D2A, CDCA7, CLP1, CNTNAP2, CTC1, CUL4B, DCX, DLG3, DNMT3B, EIF2AK3, EIF2B1, EIF2B2, EIF2B3, EIF2B4, EIF2B5, ELP1, EMD, FGD1, FMR1, FTSJ1, HELLS, IGHMBP2, IL1RAPL1, INPP5E, KCTD7, KDM5C, L1CAM, LMNA, LPAR6, LRPPRC, MED17, MEFV, MEGF8, MID1, MLC1, MRE11, NDRG1, NHEJ1, NONO, OPHN1, PAK3, PHF8, PQBP1, PUS1, SH3TC2, SLC12A6, SLC1A4, SMARCAL1, SYN1, SYNE4, THOC2, UPF3B, VPS13A, VPS13B, ZDHHC9, ZNF469, ZNF711 Intellectual disability, autism spectrum disorders, epilepsy, leukodystrophies, spastic paraplegias, ataxias, and other neurological conditions affecting brain development and function
Connective Tissue & Skeletal Disorders ADAMTS2, ALMS1, BMPER, COL11A2, COL17A1, COL27A1, COL4A3, COL4A4, COL4A5, COL7A1, CRTAP, CUL7, DDR2, DLL3, EDA, EFEMP2, EVC, EVC2, GDF5, GRIP1, KIF14, LAMA2, LAMA3, LAMB3, LAMC2, LARS, LTBP4, MESP2, OBSL1, P3H1, PLOD1, PLOD2, PLP1, PRICKLE1, SERPINF1, TNXB, WISP3, WNT1, WNT10A Ehlers-Danlos syndromes, osteogenesis imperfecta, chondrodysplasias, epidermolysis bullosa, Alport syndrome, and other connective tissue and skeletal disorders
Primary Immunodeficiencies AK2, BTK, CD247, CD3D, CD3E, CD3G, CD40LG, CD59, CD8A, CIITA, CORO1A, DCLRE1C, DOCK8, FOXN1, FOXP3, IKBKB, IL2RA, IL2RG, IL7R, JAK3, LCK, LIG4, MALT1, NDUFA11, NDUFAF2, NDUFAF5, NDUFS4, NDUFS6, NDUFS7, NDUFV1, PRF1, PRKDC, PTPRC, RAG1, RAG2, RFX5, RFXANK, RFXAP, SNX10, SP110, STK4, STX11, STXBP2, UNC13D, WAS, ZAP70 Severe combined immunodeficiency (SCID), X-linked agammaglobulinemia, chronic granulomatous disease, Wiskott-Aldrich syndrome, and other primary immunodeficiency disorders
Kidney & Urinary Tract Disorders AGPAT2, AQP2, ATP6V0A2, ATP6V0A4, ATP6V1B1, ATP6V1E1, AVPR2, CLCN5, CLCNKB, GNPAT, GNPTAB, GNPTG, INVS, KCNJ1, KCNJ11, LMAN1, LMBRD1, NPHP1, NPHP3, NPHS1, NPHS2, OCRL, PKHD1, SLC4A11, VDR, VLDLR Polycystic kidney disease, nephrotic syndrome, renal tubular acidosis, Dent disease, Bartter syndrome, Gitelman syndrome, and other kidney disorders
Endocrine Disorders AMH, AMHR2, AR, CASR, CYP11A1, CYP11B1, CYP11B2, CYP17A1, CYP19A1, CYP1B1, CYP21A2, CYP27A1, CYP27B1, CYP4F22, CYP7B1, DUOX2, DUOXA2, GHR, GHRHR, GNRHR, IYD, LHX3, LIFR, NR0B1, POU1F1, POU3F4, PROP1, SRD5A2, ST3GAL5, STAR, TBX19, TCIRG1, TPO, TRHR, TSHB, TSHR Congenital adrenal hyperplasia, disorders of sex development, congenital hypothyroidism, growth hormone deficiency, and other endocrine disorders
Ciliopathies & Cell Biology Disorders B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BSND, CASQ2, CCDC103, CCDC151, CCDC39, CCDC8, CCDC88C, CEP104, CEP152, CEP290, MKKS, MKS1, RSPH9, SDCCAG8, TCTN1, TCTN2, TCTN3, TMEM138, TMEM216, TMEM231, TMEM237, TMEM38B, TMEM67, TMEM70, DNAH5, DNAI1, DNAI2, DNAL1, DYNC2H1, HYLS1, SPATA7, RAB23, IFT140, TRAPPC11 Bardet-Biedl syndrome, Joubert syndrome, Meckel syndrome, nephronophthisis, primary ciliary dyskinesia, and other ciliopathy disorders
Cancer Predisposition & DNA Repair ATM, BLM, BRIP1, DDB2, ERCC2, ERCC3, ERCC4, ERCC5, ERCC6, ERCC8, FANCA, FANCB, FANCC, FANCD2, FANCE, FANCF, FANCG, FANCI, FANCL, LYST, MRE11, NBN, POLG, POLH, POLR1C, RNASEH2A, RNASEH2B, RNASEH2C, TREX1, WRN, XPA, XPC, ZBTB24 Fanconi anemia, xeroderma pigmentosum, Bloom syndrome, ataxia-telangiectasia, and other DNA repair disorders that predispose to cancer
Peroxisomal Disorders PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7, GNPAT Zellweger spectrum disorders, rhizomelic chondrodysplasia punctata, and other peroxisome biogenesis disorders
Other Genetic Conditions ADK, ANO10, ANO5, AP1S1, AP1S2, AP3B1, AP3D1, APOPT1, ARL13B, ARL6, BLOC1S3, BLOC1S6, BMP1, C19orf12, C8orf37, CAD, CAVIN1, CHMP1A, CLCF1, CLN3, CLN5, CLN6, CLN8, COASY, CPLANE1, CRLF1, DCAF17, DDX11, DOLK, DTNBP1, EXOSC3, FRAS1, FREM2, GORAB, LDLR, LDLRAP1, LPL, LRP2, MANBA, MAN2B1, MCPH1, MFSD8, NIPAL4, NTRK1, OSTM1, PIP5K1C, PIGN, PLA2G6, PNPLA1, POC1A, PPIB, RMRP, ROGDI, SDR9C7, SELENON, SEPSECS, SGP11, SGP21, SGP7, SKIV2L, SLC2A10, SLC2A2, SNAP29, SPG11, SPG21, SPG7, SPINK5, TBCE, TECPR2, TNFSF11, TRDN, TRIM32, TRIM37, TRMU, TRPM6, TSEN2, TSEN34, TSEN54, TSFM, TTC37, TTC7A, TTC8, TULP1, VPS45, VPS53, VRK1, VSX2, AMPD2, ERBB3 Various rare genetic disorders including mitochondrial disorders, neuronal ceroid lipofuscinoses, spastic paraplegias, and other miscellaneous genetic conditions

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.

How DNA Sequencing Works

DNA is broken into small fragments, sequenced, and computationally assemble into the full genome.

What is Sequencing Depth?

Sequencing depth is how many times your DNA is read. Higher depth = more accurate results, lower depth = risk of missed mutations.

Genome Size Matters!

Larger genomes (like humans) need more sequencing reads. That’s why high-depth testing matters—it ensures nothing is missed.

Why Jeen?

Not all genetic tests are created equal. At Jeen, we use 50x sequencing coverage, which means each section of your DNA is read around 50 times. Here’s why it makes a difference:

Bigger genome → more data needed

Higher depth → better accuracy

Balance cost vs. detail!

What Now?

Have questions? We’re here to help. Genetic testing can feel overwhelming—but it doesn’t have to be. Our NHS-trained genetic counsellors are here to walk you through your options, explain the science in plain English, and help you decide if testing is right for you.

Genetics 101

Watch Ailidh Watson's, our genetic counsellor lead, video on what genetics is.

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.

NIPT Testing Options

NIPT gives you a safe and early look at your baby’s health – explore the conditions we can screen for during pregnancy

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 Specialists 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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Thank you

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