PrenatalSafe® 5
Trisomies 21 (Down's), 18 (Edwards'), 13 (Patau's) plus sex-chromosome conditions; optional fetal sex.
Reassurance, early and safely. PrenatalSafe® analyses placental DNA from a simple maternal blood sample — from 10 weeks, with genetic counselling included.
Trisomies 21 (Down's), 18 (Edwards'), 13 (Patau's) plus sex-chromosome conditions; optional fetal sex.
Every chromosome, rarer trisomies (9, 16, 22), structural changes and the 9 most common microdeletion syndromes.
Karyo Plus plus single-gene screening: 25 de novo genes (44 conditions), cystic fibrosis, sickle cell, beta thalassaemia, hereditary deafness.
Every test includes a GP pre-test call, accredited laboratory analysis, geneticist counselling and free RhSafe® (baby's Rhesus D group). Twin surcharge confirmed at booking. Member rates do not apply to NIPT.
T21 (Down's syndrome), T18 (Edwards'), T13 (Patau's), sex-chromosome conditions and fetal sex. Advanced packages add microdeletions, genome-wide analysis and single-gene conditions.
Every test includes genetic counselling before and after, plus dedicated support if you receive a high-chance result. NIPT is a screening test — a high-chance result is not a diagnosis, and we'll guide you through the next steps with no pressure.
Most findings are minor. If anything needs a closer look we contact you promptly — at no extra charge — explain what it means, arrange any onward investigation, and can liaise with your NHS GP.
Using private medical insurance? We can provide an itemised invoice in your insurer's preferred format — please check your policy first.
See all prices — download our Services & Pricing 2026 (PDF) →
Book online, call 01772 282189, or email us. Open Mon–Fri 8:30–18:00, Sat 9:00–13:00. A £25 prepayment secures your appointment and is fully deducted from your final fee.
Safe from 10 weeks. Genetic counselling included before and after your test.