Carrier Screening Test in Royal Tunbridge Wells

Name: Carrier Screening in Royal Tunbridge Wells
Brand: Jeen Health
SKU: CARRIER-SINGLE-SWAB

Carrier screening in Royal Tunbridge Wells - what to expect locally

Carrier screening in Royal Tunbridge Wells checks 1,008 genes linked to inherited recessive conditions. Many of these conditions develop when a child inherits a change in the same gene from both parents, who are usually healthy carriers themselves; others, such as X-linked conditions, follow a different pattern. Carriers often have no family history of the condition, so most people only find out they are carriers by being tested. Testing before pregnancy, or early in one, gives you the most options.

You can collect your sample at home with an oral swab or the Tasso Home Collection Kit, have your blood taken at a Jeen partner clinic, or book a home-nurse visit. Where we have a partner clinic in or near Royal Tunbridge Wells, it is listed with its address in the Clinic network section further down this page.

Before you test you have a 30-minute consultation with a Jeen genetic counsellor (video or phone), included in the price. Results take 17-21 working days from when the laboratory receives your sample. Your genetic counsellor reviews your result, and we book a follow-up consultation if it is high-risk. If you are planning a pregnancy together, the couple option screens both of you.

Carrier screening is a screening test, not a diagnosis. No panel detects every variant, so a negative result lowers but does not remove the chance that you are a carrier, and some results are variants of uncertain significance. What a result means for a pregnancy depends on the gene, how it is inherited and, for many conditions, whether your partner is also a carrier.

Saliva or blood? How the two sample types compare.

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 consent form is signed. Changed your mind? Return the kit unused within 30 days at no charge.

2. Posting your sample back. 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 at a Jeen partner clinic or by a mobile phlebotomist - or, with the Tasso Home Collection Kit, a blood sample you collect yourself at home and post back.

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.

Price, turnaround and coverage side by side.

Test

From

Turnaround

Coverage

Price

Sperm Analysis in London

2-3 working days

£220

Karyotype Chromosome Analysis

Newborn Genetic Screening

3-4 weeks

258 genes

£720

Carrier Screening + Karyotype

17-21 working days

£870

CGT - Igenomix Carrier Genetic Test

25 working days

£990

Clinic network

1 location in Royal Tunbridge Wells

Visit our partner clinic in Royal Tunbridge Wells for a quick blood draw - no appointment hassle.

Tunbridge Wells

77 Mount Pleasant Road, Tunbridge Wells, TN1 1PX

Location

+£40

Add-on cost

Avg booking

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Tasso Home Collection Kit

How to collect blood with the Tasso device

The Tasso device is a small, single-use kit that collects a blood sample from your upper arm without a needle in your vein. A gentle button-press opens tiny channels just under the skin, and the sample is drawn into a collection tube. It takes a few minutes at home - no clinic visit, no phlebotomist. Follow the four steps below to collect your sample correctly.

1
Attach the collection tube

Take the green-capped collection tube from your kit and attach it to the base of the Tasso device until it clicks into place.
2
Place on your shoulder and activate

Press the device firmly onto your clean, dry upper shoulder so it sticks, then press the red button to begin collection. Keep it in place and let the tube fill.
3
Check the blood level, then remove the tube

The blood level must reach at least another 200 above the 400 mark on the tube - fill close to the top, but do not overfill. Once there is enough blood, remove the collection tube from the device.
4
Close, shake and prepare for return

Close the green cap securely and shake the tube gently to mix. Complete the label, seal the tube inside the biohazard bag, and return it using the prepaid packaging in your kit. Don't forget to include your completed test requisition form in the box.

Post it back any day of the week. Your results take the same time as with our other collection methods - the Tasso kit is simply another way to give your sample at home.

Please note: the Tasso blood collection device may very rarely leave a permanent mark of approximately 2 mm on the shoulder. Although the mark is usually barely visible, please consider this before selecting this blood collection option.

FAQ

Frequently asked questions.

How much does carrier screening cost in Royal Tunbridge Wells?

Carrier screening in Royal Tunbridge Wells 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 pre-test genetic-counsellor consultation.

Where can I take a carrier-screening test in Royal Tunbridge Wells?

You can collect your sample at home with our oral-swab kit (included in the price) or the Tasso Home Collection Kit (+£25 for one person, +£50 for a couple), have your blood drawn at a Jeen Clinic Network partner clinic (+£40 for one person, +£80 for a couple), or book a home-nurse visit (+£65 for one person, +£130 for a couple). Partner clinics near Royal Tunbridge Wells, where we have them, are listed in the Clinic network section of this page. Any kit is dispatched by next-day delivery after your pre-test consultation and once your consent form is signed.

How long do carrier-screening results take in Royal Tunbridge Wells?

Reports take 17-21 working days from the date the lab receives your sample. Each result is reviewed by your genetic counsellor; we book a follow-up consultation if findings are high-risk.

Should I do carrier screening in Royal Tunbridge Wells 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.

Do I need a GP referral for carrier screening in Royal Tunbridge Wells?

No. Anyone aged 18+ can book directly with Jeen Health, with no GP referral. After you order we email you a link to book your included 30-minute pre-test consultation with a genetic counsellor (video or phone). Your kit is dispatched by next-day delivery once that consultation is done and your consent form is signed.

What can carrier screening not tell me?

Carrier screening is a screening test, not a diagnosis. No panel detects every variant in every gene, so a negative result lowers but does not remove the chance that you are a carrier, and some results are variants of uncertain significance. It cannot tell you whether a pregnancy will be healthy, and what a result means for a pregnancy depends on the gene, how it is inherited and, for many conditions, whether your partner is also a carrier.

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 acidaemias, 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

Haemoglobinopathies (sickle cell disease, thalassaemias), bleeding disorders (haemophilia), platelet disorders, iron metabolism disorders, and other haematological 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, colour 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 agammaglobulinaemia, 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 anaemia, 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

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Carrier Screening in Royal Tunbridge Wells

Who's testing?

Choose your collection method

Your partner's details

Carrier screening in Royal Tunbridge Wells - what to expect locally

The logistics, simply.

Kit delivery & logistics

Sample / draw options

Test suitability

Three steps. That's it.

Talk to a clinician

Consent + collect

Results + follow-up

Compare every option we offer.

1 location in Royal Tunbridge Wells

How to collect blood with the Tasso device

Attach the collection tube

Place on your shoulder and activate

Check the blood level, then remove the tube

Close, shake and prepare for return

Frequently asked questions.

How much does carrier screening cost in Royal Tunbridge Wells?

Where can I take a carrier-screening test in Royal Tunbridge Wells?

How long do carrier-screening results take in Royal Tunbridge Wells?

Should I do carrier screening in Royal Tunbridge Wells before pregnancy?

Do I need a GP referral for carrier screening in Royal Tunbridge Wells?

What can carrier screening not tell me?

All 1,008 genes by category

Talk to a specialist.