1 / 6 VeriSeq v2 NIPT
Non-invasive prenatal screen from 10 weeks, analysed on Illumina's VeriSeq v2 platform at TDL Genetics in the UK. Screens the 3 most common chromosomal conditions plus optional fetal sex, with a 3-4 working day turnaround.
Analysed on Illumina's VeriSeq v2 platform at TDL Genetics (The Doctors Laboratory) in the UK
Detection rate >99% for Down's syndrome (trisomy 21; a screening test, not a diagnosis); optional fetal sex reporting
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.
The logistics, simply.
Everything you need to know about shipping, blood draw, and suitability.
Kit delivery & logistics
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.
Sample / draw options
Sample / draw options
Maternal blood draw : A standard blood draw from the pregnant person - no risk to the pregnancy.
Test suitability
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.
Three steps. That's it.
Simple, clinician-supported steps to take your test with Jeen.
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.
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 midwife. We share them with you securely, and book a follow-up consultation with onward referrals if your result is high-risk.
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.
200+ collection points across the UK
If you choose a clinic blood draw, you can pick a collection point near you on the map.
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Partner clinics are also listed below. How we use cookies
Frequently asked questions.
How much does VeriSeq v2 NIPT cost?
When can I take VeriSeq v2 NIPT during pregnancy?
What conditions does VeriSeq v2 NIPT screen for?
How accurate is VeriSeq v2 NIPT?
Who runs the VeriSeq v2 analysis, and how fast are results?
Do I need a GP or hospital referral for VeriSeq v2 NIPT?
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).
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 consultationQuick check before you order
Three short questions so the lab can run NIPT reliably - every NIPT panel needs a pregnancy of adequate gestational age, confirmed by a recent scan, before a sample is taken. Suitable for singleton pregnancies. If you are expecting twins or have used donor eggs or a surrogate, please speak to our midwife before ordering.
Book a scan with London Pregnancy Clinic or email [email protected] or WhatsApp us if you need help.