1 / 6

Carrier Screening in Cardiff

Patient reviews

Carrier Screening in Cardiff

Name: Carrier Screening in Cardiff
Brand: Jeen Health
SKU: CARRIER-SINGLE-SWAB

£660 See variants below

Carrier screening in Cardiff 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?

Single £660 Couple £1,200

Choose your collection method

Klarna's credit agreements are not regulated by the FCA. Use of these and any missed payments may affect your ability to obtain credit from Klarna and other lenders. 18+, UK residents only. Subject to status. T&Cs apply. Klarna terms apply.

● In stock · Secure checkout via Stripe

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 Cardiff - what to expect locally

We collect your sample at a partner clinic in the city centre, a few minutes from Cardiff Central for easy access. Cardiff and the wider South Wales region have one of the highest cystic-fibrosis carrier rates in the UK.

Carrier screening in Cardiff 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 Cardiff 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.

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.

Consent + collect

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

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.

Reproductive & Newborn options

Compare every option we offer.

From the basic panel to our most advanced option.

Test

From

Turnaround

Conditions

Price

Sperm Analysis in London

2-3 working days

£220

Karyotype Chromosome Analysis

Newborn Genetic Screening

3-4 weeks

258

£720

Carrier Screening + Karyotype

17-21 working days

£870

CGT - Igenomix Carrier Genetic Test

25 working days

£990

Clinic network

2 locations in Cardiff

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

Cardiff

Holland & Barrett, Unit 4, 53-57 Queen Street, St Davids Centre, Cardiff, CF10 2AS
Creigiau Pharmacy

69 Parc Y Bryn Creigiau, Cardiff, CF15 9SE

Locations

+£40

Add-on cost

Avg booking

This map is served by Google Maps, which sets its own cookies on your device.

Clinic addresses are listed below too. How we use cookies

FAQ

Frequently asked questions.

How much does carrier screening cost in Cardiff?

Carrier screening in Cardiff 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 Cardiff?

You can complete your sample at home in Cardiff using our free oral-swab kit (posted next-day), at the Jeen Clinic Network in Cardiff 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 Cardiff?

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 Cardiff 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 Cardiff regularly book the couple test together in one consultation.

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

No. Anyone aged 18+ can book directly with Jeen Health. Your kit will arrive in Cardiff 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

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 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

GNPAT, PEX1, PEX10, PEX11B, PEX12, PEX13, PEX14, PEX16, PEX19, PEX2, PEX26, PEX3, PEX5, PEX6, PEX7

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

Get in touch