1 / 6 Niptify NIPT
Non-invasive prenatal screen from 10 weeks. 33 conditions, 5–10 day turnaround.
Mid-range 33-condition panel
From 10 weeks of pregnancy
Free midwife consultation before you take the test
Optional fetal sex reveal with >99% accuracy
Common NIPT questions, and what a positive result really means.
- Down's Syndrome (Trisomy 21)
- Edwards' Syndrome (Trisomy 18)
- Patau's Syndrome (Trisomy 13)
- Rare autosomal trisomies and monosomies (genome-wide)
- DiGeorge Syndrome (22q11.2 deletion)
- Prader–Willi / Angelman Syndrome
- Williams–Beuren Syndrome
- 1p36 Deletion Syndrome
- Cri-du-Chat Syndrome
- Wolf–Hirschhorn Syndrome
- Jacobsen Syndrome
- Langer–Giedion Syndrome
- Duchenne Muscular Dystrophy
- Smith–Magenis Syndrome
- 15q11-q13 Duplication Syndrome
- Neurofibromatosis Type 1
- Koolen-De Vries Syndrome (17q21.31 deletion)
- Phelan–McDermid Syndrome
- Miller–Dieker Syndrome
- Pallister–Killian Syndrome
- 3q29 Deletion Syndrome
- 2q31.2 Deletion Syndrome
- 15q24 Deletion Syndrome
- 17q12 Deletion Syndrome
- 7q11.23 Duplication Syndrome
- additional genome-wide CNVs >1 Mb
- m.1095T>C
- m.1494C>T
- m.1555A>G(associated with sensorineural hearing loss)
- Segmental aneuploidies in chromosomes 13, 18, 21
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 free 20-minute specialist midwife consultation 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.
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 and twin pregnancies, including IVF pregnancies (both own-egg and egg-donor). Best performed between from 10 weeks 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 free 20-minute consultation with our specialist midwife. 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 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 our most advanced option.
200+ collection points across the UK
A simple, low-cost option with flexible scheduling. For many patients, this is the quickest and most practical way to complete the test.
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Frequently asked questions.
How much does Niptify NIPT cost?
When can I take Niptify NIPT during pregnancy?
What conditions does Niptify NIPT screen for?
How accurate is Niptify NIPT?
Do I need a GP or hospital referral for Niptify 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 add the published birth prevalence of each condition (or condition class) and express the total as "1 in N". The three autosomal trisomies are anchored to NCARDRS England 2022.
This panel:
- Trisomy 21 / 18 / 13 - 42.3 per 10,000 combined (≈1 in 240)
- Sex-chromosome aneuploidies (Turner, Klinefelter, Triple-X, XYY), combined - ~17 per 10,000 (≈1 in 580)
- 22q11.2 deletion (DiGeorge syndrome) - ~3.3 per 10,000 (≈1 in 3,000)
- ~20 further microdeletion/CNV syndromes plus genome-wide copy-number changes >1 Mb, combined - ~10 per 10,000
- Rare genome-wide trisomies/monosomies, segmental and mitochondrial changes (residual at birth) - ~2 per 10,000
Combined: ~75 per 10,000 births ≈ 1 in 130.
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); sex-chromosome aneuploidies - newborn cytogenetic surveys (e.g. Nielsen & Wohlert 1991); microdeletions/CNVs - GeneReviews / Orphanet.
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 confirmed singleton or twin pregnancy of adequate gestational age before a sample is taken.
Book a scan with London Pregnancy Clinic or email my@jeen.health or WhatsApp us if you need help.