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Carrier Screening in London
Patient reviews

Carrier Screening in London

£660 See variants below

Carrier screening in London from £660 (couple £1,200). 1,008-gene panel, free pre-test counsellor consultation, oral-swab or local clinic blood draw, results in 17–21 days.

Turnaround time 17-21 working days
Population 90%
Most advanced labs Accurate testing →

Who's testing?

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30-minute genetic counselling included with every test

NHS Genomic Medicine Service-aligned variant interpretation

At-home buccal swab included; an in-clinic blood draw is available (+£40)

Results within 17-21 working days of sample receipt

Carrier screening in London - what to expect locally

We collect your sample at our central London partner clinic, just off Marylebone Road, around the corner from Harley Street and three minutes from Oxford Circus for easy access. London families weighing genetic options often have the broadest cultural-heritage diversity in the UK, which is why our 600+ panel was developed for the city in the first place.

Carrier screening in London tests you for over 600 recessive genetic conditions - diseases that can be inherited by children when both parents carry the same gene variant, even though neither parent is affected. Most carriers don't know they're carriers, which is why pre-conception or early-pregnancy screening is the only reliable way to find out before it matters clinically.

Each London customer's report includes a one-to-one consultation with a Jeen genetic counsellor, who walks through the results in plain English and explains what the findings mean for your specific situation - whether you're planning a pregnancy, already pregnant, or weighing IVF options. We never send results without that conversation. Sample collection takes about 15 minutes; results return within 3–4 weeks. Couples often book the couple-screening package together for a more complete picture.

Saliva or blood? The same DNA, the same accuracy.

Useful information

The logistics, simply.

Everything you need to know about shipping, blood draw, and suitability.

Kit delivery & logistics

1. Get your kit from us. Free delivery of your test kit, dispatched by next-day delivery after your included 30-minute genetic counsellor consultation (video or phone) and once your test choice is confirmed. Changed your mind? Return the kit unused within 30 days at no charge.

2. Easy returns. After sample collection, send your sample in the pre-paid bag to the nearest depot (details in your email). Turnaround is counted in working days from when your sample reaches the laboratory.

Turnaround
17-21 working days

Sample / draw options

At-home cheek swab : At-home cheek swab kit; you collect the sample yourself and post it back.

Blood draw : Standard venous blood draw, performed at a clinic or by a mobile phlebotomist.

Test suitability

Genetic testing with Jeen Health is suitable for adults who have completed a pre-test consultation with one of our genetic counsellors - in clinic, over video, or by phone.

Genetic testing with Jeen Health is only available to individuals aged 18 and over.

How it works

Three steps. That's it.

Simple, clinician-supported steps to take your test with Jeen.

01

Talk to a clinician

Book your included 30-minute consultation with our genetic counsellor (video or phone). Confirm the test that's right for you.

02

Consent + collect

Complete your consent form online, receive your kit, and collect your sample at home or via a clinic of your choice.

03

Results + follow-up

Your results are reviewed by your genetic counsellor. We share them with you securely, and book a follow-up consultation with onward referrals if your result is high-risk.

Clinic network

25 locations in London

25 Jeen partner clinics in London where you can have your blood drawn. Pick the one closest to you on the map below.

  • Bliss Chemist

    50-56 Willesden Lane, London, NW6 7SX

  • Britannia Pharmacy

    Unit 9 asda centre, 151 E Ferry Road, London, E14 3BT

  • Britannia Pharmacy

    429-431 HIGH ROAD, WOODFORD GREEN, ILFORD, LONDON, IG8 0XE

  • Britannia Pharmacy

    13-15 Faircross Parade, London, IG11 8UN

  • Britannia Pharmacy

    414-416 Green Lane, London, IG3 9JX

  • Britannia Pharmacy

    167-169 High Road, Chadwell Heath, London, RM6 6NL

  • + 19 more on the map
25
Locations
+£40
Add-on cost
2d
Avg booking

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FAQ

Frequently asked questions.

How much does carrier screening cost in London?

Carrier screening in London starts at £660 for a single person and £1,200 for a couple. Both include our 1,008-gene panel covering metabolic, neuromuscular, neurological, sensory and rare-disease categories, plus a free pre-test genetic-counsellor consultation.

Where can I take a carrier-screening test in London?

You can complete your sample at home in London using our free oral-swab kit (posted next-day), at the Jeen Clinic Network in London for a blood draw (+£40), or via a home-nurse visit (+£65). Couple options include sample collection for both partners.

How long do carrier-screening results take in London?

Reports take 17–21 days from the date the lab receives your sample. Each result is reviewed by our clinical-genetics team and shared in a follow-up consultation.

Should I do carrier screening in London before pregnancy?

Yes - pre-conception is when carrier screening is most useful. Identifying recessive conditions you and your partner both carry lets you make informed decisions about family planning, IVF with PGT-M, donor selection, or early prenatal monitoring. The earlier you have the information, the more options you have. Couples in London regularly book the couple test together in one consultation.

Do I need a GP referral for carrier screening in London?

No. Anyone aged 18+ can book directly with Jeen Health. Your kit will arrive in London within one working day, and our genetic counsellor will be in touch to schedule your free pre-test consultation.
Panel composition

All 1,008 genes by category

Genes grouped by the clinical area they're associated with. Click any underlined symbol to read the gene's plain-English overview on Jeen Library - or browse per-gene carrier frequencies for population-stratified rates.

Gene category
Associated genes
Conditions
Metabolic Disorders 273 genes
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, FBP1, FBXL4, 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, and other metabolic conditions
Blood & Coagulation Disorders 28 genes
CDAN1, EPB42, F11, F2, F5, F7, F8, F9, GP1BA, GP9, HAMP, HBA1, HBA2, HBB, HFE, HJV, ITGA2B, ITGA6, ITGB3, ITGB4, MPL, NBEAL2, NBN, NCF2, NCF4, PGM3, RHAG, SEC23B
Hemoglobinopathies (sickle cell disease, thalassemias), bleeding disorders (hemophilia), platelet disorders, iron metabolism disorders, and other hematological conditions
Neuromuscular Disorders 31 genes
CAPN3, CASP14, CHAT, CHRNE, CHRNG, CLCN1, COLQ, DMD, DOK7, DYSF, ESCO2, FHL1, FKBP10, FKRP, FKTN, MTM1, MTMR2, NEB, PLEKHG5, POMGNT1, POMT1, POMT2, RAPSN, SELENON, SGCA, SGCB, SGCD, SGCG, SLC5A7, SMN1, TAZ
Muscular dystrophies (Duchenne, Becker, limb-girdle), congenital myopathies, spinal muscular atrophy, myasthenic syndromes, and neuromuscular junction disorders
Sensory Disorders (Hearing & Vision) 53 genes
ABCA4, AIPL1, CDH23, CERKL, CHM, CHST6, CIB2, CLRN1, CNGA1, CNGA3, CNGB1, CNGB3, CRB1, 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, SLC26A4, TMPRSS3, USH1C, USH1G, USH2A, WHRN
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 68 genes
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 39 genes
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 46 genes
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 26 genes
Polycystic kidney disease, nephrotic syndrome, renal tubular acidosis, Dent disease, Bartter syndrome, Gitelman syndrome, and other kidney disorders
Endocrine Disorders 36 genes
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 44 genes
B9D1, B9D2, BBS1, BBS10, BBS12, BBS2, BBS4, BBS5, BBS7, BBS9, BSND, CASQ2, CCDC103, CCDC151, CCDC39, CCDC8, CCDC88C, CEP104, CEP152, CEP290, DNAH5, DNAI1, DNAI2, DNAL1, DYNC2H1, HYLS1, IFT140, MKKS, MKS1, RAB23, RSPH9, SDCCAG8, SPATA7, TCTN1, TCTN2, TCTN3, TMEM138, TMEM216, TMEM231, TMEM237, TMEM38B, TMEM67, TMEM70, TRAPPC11
Bardet-Biedl syndrome, Joubert syndrome, Meckel syndrome, nephronophthisis, primary ciliary dyskinesia, and other ciliopathy disorders
Cancer Predisposition & DNA Repair 33 genes
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 15 genes
Zellweger spectrum disorders, rhizomelic chondrodysplasia punctata, and other peroxisome biogenesis disorders
Other Genetic Conditions 329 genes
A4GALT, AARS2, ABAT, ABCC2, ABCC6, ABCG5, ACAD8, ACP5, ACSL4, ADA2, ADAMTS13, ADAMTSL4, ADK, AGRN, AICDA, AIFM1, AIMP2, ALG13, AMPD2, ANO10, ANO5, AP1S1, AP1S2, AP3B1, AP3D1, AP4M1, APOPT1, ARHGEF9, ARL13B, ARL2BP, ARL6, ARNT2, ASAH1, ATP13A2, ATP1A2, ATP5MD, ATP6AP1, ATP8A2, B3GALT6, B4GALT1, BCAP31, BLOC1S3, BLOC1S6, BMP1, BRAT1, C19orf12, C19orf70, C2CD3, C8orf37, CAD, CAVIN1, CCDC174, CD40, CENPJ, CEP120, CEP41, CERS3, CFH, CFTR, CHMP1A, CHRNB1, CLCF1, CLN3, CLN5, CLN6, CLN8, CLRN2, COA7, COASY, COG5, COG6, COG7, COL11A1, COL6A2, CPLANE1, CRB2, CRLF1, CSPP1, CTPS1, CWC27, DCAF17, DDHD2, DDRGK1, DDX11, DEGS1, DGAT1, DIAPH1, DIS3L2, DKC1, DNAH11, DOLK, DPAGT1, DSE, DTNBP1, ECEL1, EIF2AK4, EML1, EOGT, EPCAM, EPG5, ERBB3, ERCC6L2, EXOSC3, FAM126A, FANCM, FAT4, FBXO7, FERMT1, FOXI1, FRAS1, FREM2, FRMD4A, FRMPD4, FRRS1L, GATC, GCH1, GCSH, GFM1, GH1, GJC2, GLE1, GMPPA, GORAB, GPHN, HBD, HIKESHI, HMOX1, HNRNPH2, HPRT1, HSPD1, IFNAR1, IFT172, IFT27, IGSF1, IL10RA, INSR, IQCB1, ISPD, ITPR1, KCNJ10, KIAA0586, KPTN, KRT14, KY, LAMP2, LARGE1, LARP7, LCA5, LDLR, LDLRAP1, LIPH, LONP1, LPL, LRBA, LRP2, LTBP3, MADD, MAN1B1, MAN2B1, MANBA, MBTPS2, MCPH1, MECP2, MECR, MED25, MFSD8, MGP, MOCS1, MOCS2, MPDU1, MSN, MUSK, MYBPC1, MYO15A, MYO18B, NARS2, NBAS, NCF1, NDE1, NDUFAF6, NDUFB11, NDUFS2, NEK8, NIPAL4, NPHP4, NSMCE3, NTRK1, NUP188, NUP62, ORC4, OSTM1, OTOA, OTUD6B, PAX7, PCDH12, PCNT, PDE6G, PDX1, PGAP3, PGM1, PIDD1, PIGA, PIGN, PIGQ, PIGS, PIGT, PIP5K1C, PKLR, PLA2G6, PLAA, PLCE1, PLD1, PNPLA1, POC1A, POLR3B, POMGNT2, POR, PPIB, PPP1R13L, PRDM12, PREPL, PYCR1, RARS2, RASGRP1, RAX, RBL2, RBM10, RECQL4, RMRP, ROGDI, RPL10, RPS6KA3, RXYLT1, RYR1, SASH3, SCAPER, SCARB2, SCN9A, SDHA, SDR9C7, SELENOI, SELENON, SEPSECS, SGP11, SGP21, SGP7, SGSM3, SKIV2L, SLC18A3, SLC29A3, SLC2A10, SLC2A2, SLC30A9, SLC35A2, SLC38A8, SLC4A4, SLC6A9, SNAP29, SPATA5, SPEG, SPG11, SPG21, SPG7, SPINK5, STAT1, STS, SZT2, TAF2, TANGO2, TBCB, TBCD, TBCE, TCN2, TECPR2, TECRL, TFE3, TFRC, THG1L, TIMM50, TJP2, TKT, TMC1, TMEM107, TMEM94, TNFRSF9, TNFSF11, TNNT1, TNR, TRAF3IP1, TRAPPC6B, TRDN, TRIM32, TRIM37, TRIP11, TRMU, TRPM6, TSEN2, TSEN34, TSEN54, TSFM, TSPEAR, TTC37, TTC7A, TTC8, TULP1, TWNK, UBA1, UBR1, UNC80, UNG, UPB1, UQCRQ, USP9X, VPS11, VPS37A, VPS45, VPS53, VRK1, VSX2, WDPCP, WDR34, WDR62, WWOX, XRCC2, YARS, ZFYVE26, ZIC3, ZNF341, ZNHIT3
Various rare genetic disorders including mitochondrial disorders, neuronal ceroid lipofuscinoses, spastic paraplegias, and other miscellaneous genetic conditions
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