Testing for >1000 conditions using your DNA
Speak to a Genetic Counsellor Today

Cancer Genetic Testing

Get personalised genetic testing and counselling for hereditary cancers with expert private cancer screening in UK.

Use responsibly. T&Cs & late fees apply at clearpay.co.uk/terms

Why genetics?

At Jeen, we believe knowledge is power — and your DNA holds vital information about your health. Our mission is to make genetic testing simple, accessible, and meaningful for everyone. By combining expert guidance with at-home convenience, we empower you to understand your inherited risks and take control of your future health.

Cancer Test options

Cancer Screening

Turnaround

17

-

21

days

Variants
50
Book £
660

Breast Cancer Screening

Turnaround

17

-

21

days

Variants
13
Book £
660

Prostate Cancer Screening

Turnaround

17

-

21

days

Variants
11
Book £
660

Ovarian Cancer Screening

Turnaround

17

-

21

days

Variants
13
Book £
660

Colorectal Cancer Screening

Turnaround

17

-

21

days

Variants
14
Book £
660

Pancreatic Cancer Screening

Turnaround

17

-

21

days

Variants
11
Book £
660

Endometrial Cancer Screening

Turnaround

17

-

21

days

Variants
7
Book £
660

BRCA Testing

Turnaround

17

-

21

days

Variants
2
Book £
660

Melanoma Skin Cancer Testing

Turnaround

17

-

21

days

Variants
5
Book £
660

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

Why Test?

In the UK, 1 in 2 people will be diagnosed with cancer at some point in their life. Genetic testing can help identify your risk of developing some of the most common types of cancer, so you can take action early.

Up to 10%

of all cancers are linked to inherited genetic changes including some of the most common gender-specific cancers like breast cancer and prostate cancer.

Genetic Counselling

The Power of Pedigree

A key part of your test is a 45-minute personalised session with one of our genetic counsellors. Genetics can be complex, but you're not alone. We're here to guide you through it. By exploring your family history, we can uncover valuable insights that could make a real difference to your health.

The Test

Cancer Focus Panel

Our genetic cancer panel focuses on 50 carefully chosen genes, all backed by strong scientific evidence. While some tests look at more genes, many include ones with little clinical value. We focus on what’s most useful, so you get results you can actually act on.

The Lab

Fulgent Genetics - Trusted Partner

Fulgent Genetics, based in California, is a global leader in genetic testing and analysis. We’ve partnered with them because quality matters, especially when it comes to your health. Their state-of-the-art Illumina sequencing technology delivers over 99% accuracy at 50x coverage, ensuring your results are both reliable and clinically meaningful.

Research

World-class experts

Medicine is always evolving and so are we. Our expert team stays up to date with the latest research and clinical guidelines, so you’re always getting advice that’s current, trusted, and tailored to you.

What's Next?

What happens if my DNA shows a higher-risk gene?

01

Genetic Counselling

Our pre-test counselling is designed to help you understnad the scope of the test and your hereditary cancer risk. Our experienced counsellors will prepare you for all the outcomes of your test.

02

Follow Up

We will offer you a complimentary consultation with our genetics clinician specialising in cancer genetics to further discuss the implications of the higher risk test result.

03

Tailored Plan

Our clinical team will create a personalised plan for you, which may include further tests or scans, along with lifestyle changes to help reduce your risk. In some cases, we may also recommend risk‑reducing surgery if it's the right option for you.

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

Our Pricing

Transparent. Personalised. No surprises.

Genetic
Counselling

Frequently Asked Questions

How is genetic testing for cancer performed?

At Jeen, our private genetic testing for cancer uses a simple cheek swab you can do at home. Your DNA is analysed in a certified lab to look for inherited changes that may increase your cancer risk.

We test for more than just cancer genes, giving you faster results and a fuller picture of your health. Whether you're in London or anywhere in the UK, our private cancer screening helps you take control of your health with expert guidance.

What cancers can be genetically tested?

If you’re looking for comprehensive genetic testing to check for inherited risks linked to breast, ovarian, prostate, bowel, pancreatic, or skin cancers, Jeen offers at-home DNA tests across the UK.

The test analyses 50 carefully chosen genes, each backed by strong scientific evidence linked to prostate cancer risk. Our testing gives you a clearer view of your genetic risk and helps you make confident, informed decisions about your health.

Can genetic testing detect cancer?

Genetic testing looks for inherited gene changes that could raise your risk of certain cancers, often before any symptoms appear.

It doesn’t detect cancer itself, but it gives you the chance to take early, proactive steps like tailored screening or prevention. With this insight, you can understand your health better and stay one step ahead.

How accurate is genetic testing for cancer?

Our genetic testing for cancer at Jeen is designed for accuracy and reliability.

Our partner lab uses advanced technology called 50x sequencing, which reads each part of your DNA about 50 times. This helps us find inherited gene changes linked to cancers like breast, ovarian, prostate, and bowel cancer.

While no test can guarantee you’ll or won’t get cancer, ours gives you trusted insights to help you plan ahead. Learn more about the statistics here at Jeen.

How long does genetic testing for cancer take?

At Jeen, your genetic testing journey takes up to four weeks from start to finish. You’ll have a consultation with a genetic counsellor, receive an at-home cheek swab kit, and send it back by post.

Your DNA is analysed in a certified lab, and results are shared with you promptly, so you can take the next steps with confidence.

Should I get tested for cancer if it runs in my family?

If cancer runs in your family, genetic testing can help uncover inherited risks you might not even be aware of. Some gene changes can skip generations or be influenced by lifestyle. Even a distant relative’s diagnosis could matter. During your appointment, we’ll go through a full family history (called a pedigree) to understand your risk in more detail. With support from Jeen’s expert genetic counsellors, you’ll get the answers you need to make informed choices and plan ahead with confidence.

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.

Check - Elements Webflow Library - BRIX Templates

Thank you

Thanks for reaching out. We will get back to you soon.
Oops! Something went wrong while submitting the form.