PrenatalSafe 3 UKPrenatalSafe 3 UK - view 2PrenatalSafe 3 UK - view 3PrenatalSafe 3 UK - view 4PrenatalSafe 3 UK - view 5PrenatalSafe 3 UK - view 6 1 / 6
PrenatalSafe 3 UK
Patient reviews

PrenatalSafe 3 UK

£325 from 10 weeks · Singleton pregnancies
200+ collection locations near you Find your nearest

Non-invasive prenatal screen from 10 weeks. 3 conditions, 2-4 working day turnaround.

Turnaround time 2-4 working days
Affects pregnancies 1 in 240*
Laboratory analysis About our testing →

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

Turnaround of 2-4 working days

Detection rate >99% for trisomy 21 (a screening test, not a diagnosis)

Midwife consultation included before you take the test (a £50 fee applies if you speak with the midwife and testing does not go ahead)

Results reviewed by your midwife; specialist follow-up if high-risk

Common NIPT questions, and what a positive result really means.

What this test screens for
3
conditions checked In a single non-invasive test
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 midwife consultation and signed consent. 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
2-4 working days
Laboratory
UK

Sample / draw options

Maternal blood draw : A standard blood draw from the pregnant person - no risk to the pregnancy.

Test suitability

Suitable for singleton pregnancies. If you are expecting twins or have used donor eggs or a surrogate, please speak to our midwife before ordering. Best performed between 10 and 16 weeks of pregnancy.

Not suitable for pregnancies beyond 16 weeks, triplet (or higher-order) pregnancies, or where the patient has a history of chromosomal abnormalities, parental mosaicism, fetal demise, an active malignancy, or a previous bone marrow / organ transplant.

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

⚠ If your pregnancy has progressed beyond 16 weeks, please reach out before booking. Our genetic counsellors will discuss your circumstances and recommend the most suitable option.

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 20-minute consultation with our specialist midwife. Confirm the test that's right for you. If you speak with the midwife but testing does not go ahead, a £50 consultation fee applies.

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 midwife. We share them with you securely, and book a follow-up consultation with onward referrals if your result is high-risk.

NIPT options

Compare every NIPT we offer.

From the basic panel to the tests that add microdeletions and single-gene conditions.

A dash means we do not state a condition total for that test; its page lists the conditions it screens for.

Clinic network

200+ collection points across the UK

If you choose a clinic blood draw, you can pick a collection point near you on the map.

200+
Partners
+£40
Add-on cost
2d
Avg booking

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

Partner clinics are also listed below. How we use cookies

FAQ

Frequently asked questions.

How much does PrenatalSafe 3 UK cost?

PrenatalSafe 3 UK starts at £325. The price includes a 20-minute midwife consultation (if you speak with the midwife but testing does not go ahead, a £50 consultation fee applies), the test kit shipped to you, lab analysis at our UK partner laboratory, and a clinical-grade report reviewed by your midwife. A specialist follow-up consultation is offered if your result is high-risk.

When can I take PrenatalSafe 3 UK during pregnancy?

PrenatalSafe 3 UK can be taken from 10 weeks. Suitable for singleton pregnancies. If you are expecting twins or have used donor eggs or a surrogate, please speak to our midwife before ordering. We also don't recommend it if you have a history of chromosomal abnormalities, parental mosaicism, fetal demise, an active malignancy, or a previous bone-marrow / organ transplant - speak with our midwife first.

What conditions does PrenatalSafe 3 UK screen for?

PrenatalSafe 3 UK screens for 3 chromosomal and genetic conditions, including Down syndrome (Trisomy 21), Edwards syndrome (Trisomy 18), Patau syndrome (Trisomy 13). It does not screen for sex-chromosome aneuploidies or microdeletions; some of our other NIPTs add those. Results are reviewed by your midwife; a specialist follow-up consultation is offered if your result is high-risk.

How accurate is PrenatalSafe 3 UK?

Detection rates exceed 99% for Down's syndrome (Trisomy 21); detection for Edwards' (T18) and Patau's (T13) is also high but somewhat lower, around 97-99%. NIPT is a screening test - high-risk results should be confirmed with a diagnostic procedure such as CVS or amniocentesis. If your result is high-risk our specialist team will book a follow-up consultation to talk you through next steps.

Do I need a GP or hospital referral for PrenatalSafe 3 UK?

No. Anyone aged 18+ can book PrenatalSafe 3 UK directly with Jeen Health. Your kit is dispatched by next-day delivery after your 20-minute midwife consultation and signed consent; your midwife reviews every report and a specialist follow-up is offered if your result is high-risk.

How we estimate "affects ~1 in N pregnancies"

The "1 in N" is an approximate UK total-birth prevalence - how often, across all births (live births plus stillbirths and terminations for fetal anomaly), a pregnancy is affected by one of the conditions this screen covers. We take the published birth prevalence of each condition, add them together, and express the total as "1 in N". The three autosomal trisomies are anchored to NCARDRS England 2022 (NHS England Digital).

This panel (3 conditions):

  • Trisomy 21 (Down's syndrome) - 30.2 per 10,000 (≈1 in 331)
  • Trisomy 18 (Edwards' syndrome) - 8.7 per 10,000 (≈1 in 1,150)
  • Trisomy 13 (Patau's syndrome) - 3.4 per 10,000 (≈1 in 2,900)

Combined: 42.3 per 10,000 births ≈ 1 in 240.

This is a population detection rate, not your personal risk - your own risk depends on maternal age, family history and other factors, and a screen result is not a diagnosis. Because each test covers a different set of conditions, the figures are not directly comparable between tests.

Sources: autosomal trisomies - NCARDRS England 2022 (NHS England Digital).

Get in touch

Talk to a specialist.

Our team is here to help. Whether you're curious about testing, your results, or what's right for you - we're a message away.

Book a consultation