NIPT

Non-Invasive Prenatal Testing

A simple maternal blood test from 10 weeks - screens for chromosomal conditions with 99%+ accuracy. Zero miscarriage risk. Results in 2-10 working days from when your sample reaches the laboratory (varies by test).

From 10 weeks 99%+ accuracy 38 UK locations
Book NIPT - From £295
Jeen NIPT - non-invasive prenatal testing
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What is NIPT?

Non-Invasive Prenatal Testing (NIPT) is a simple blood test that can give you clear information about your baby’s risk of the 3 main chromosomal conditions:

  • Down’s syndrome (Trisomy 21)
  • Edwards’ syndrome (Trisomy 18)
  • Patau’s syndrome (Trisomy 13)

It works by analysing small fragments of your baby’s DNA found in your blood. There’s no risk to your pregnancy, and results are usually available within 2-10 working days from when your sample reaches the laboratory (varies by test). We also offer extended NIPT options testing for hundreds of conditions.

Optional fetal sex reveal is available for all tests.

What if I get a Positive Result?

Chromosomes Checked

Chromosomes Checked

See full list of conditions

Down’s Syndrome

Edwards’ Syndrome

Klinefelter Syndrome

DiGeorge Syndrome

Turner’s Syndrome

Patau’s Syndrome

Triple X Syndrome

Sex Chromosome Anomalies

NIPT options

NIPT options

Trusted specialists

How it works

Chat with our specialist midwife, arrange your NIPT blood draw - your own at no extra cost, a partner collection point (+£40) or a home-nurse visit (+£65) - and get your results in 2-10 working days from when your sample reaches the laboratory.

01

Online Midwife Counselling

Speak to our specialist midwife, pick what NIPT test you want

02

Bloods Test

Arrange your own blood draw at no extra cost, or we can arrange one at a Jeen partner collection point (+£40) or a home-nurse visit (+£65)

03

Report & Recommendations

Get your detailed report and recommendations

Locations

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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Why test?

Why test?

Non-Invasive Prenatal Testing (NIPT) offers a safe, early look at your baby’s health using just a small blood sample. It screens for the most common chromosomal conditions such as Down’s syndrome and gives highly accurate results from as early as 10 weeks into pregnancy. With NIPT, you can make informed choices sooner and feel confident in the care you’re receiving throughout your pregnancy.

>99%

NIPT offers over 99% sensitivity for Down’s syndrome and significantly reduces false positives compared to traditional screening. That means fewer unnecessary invasive procedures and greater peace of mind.

Obstetric Input

The Value of Review

Before your test, our team of obstetricians and fetal medicine specialists will review your pregnancy scan report to make sure NIPT is right for you. This helps us provide results that are as accurate and helpful as possible. You’ll need to upload a pregnancy scan report showing your gestational age, from an NHS provider or a CQC-registered private ultrasound clinic. The scan must have been performed within one week of your blood draw.

Midwife Counselling

Personalised Support

Every NIPT with Jeen includes a one-to-one session with a qualified midwife from London Pregnancy Clinic. We’ll explain your options, help you choose the right panel for your needs, and support you in understanding what your results mean for you and your baby. It’s not just a test, it’s expert advice, personalised to your pregnancy.

Partner Labs

Trusted Global Leaders

We work with leading international laboratories, including Fulgent Genetics, Natera, BillionToOne, and Eurofins, to deliver the highest standards in prenatal screening. These labs use advanced next-generation sequencing and cutting-edge technology to ensure accuracy, reliability, and fast turnaround times.

Research

Driven by Science

Our team and partners stay on top of the latest clinical guidelines, emerging research, and technological advances in prenatal genetics. That means you benefit from up-to-date, evidence-based advice, delivered by experts who understand the science and support behind every test.

Our Advanced NIPT

Book a midwife counselling session first. The counselling fee counts towards the cost of your test. If you decide not to go ahead after counselling, you’ll only pay for the counselling. If you proceed, we’ll deduct the counselling fee from your test price.

Detection rates

Accuracy by condition.

Independently-published detection rates and population prevalence for each advanced panel. Tap a panel to see its full per-condition breakdown.

Panorama NIPT £375
ConditionDetectionPrevalence
Autosomal trisomies
Trisomy 21 (Down syndrome) 99.0% 1:700
Trisomy 18 (Edwards syndrome) 94.1% 1:5,000
Trisomy 13 (Patau syndrome) 99.0% 1:16,000
Sex chromosome aneuploidies
Turner syndrome (45,X) 94.7% 1:2,500
Klinefelter syndrome (47,XXY) 73.1% 1:650
Triple X syndrome (47,XXX) 73.1% 1:1,000
Jacob’s syndrome (47,XYY) 73.1% 1:1,000
Other chromosomal abnormalities
Triploidy (69,XXX/XXY/XYY) 99.0% 1:10,000
Microdeletion syndromes
DiGeorge syndrome 83.3% 1:4,000
1p36 deletion syndrome 99.0% 1:5,000
Angelman syndrome 95.5% 1:15,000
Cri-du-Chat syndrome 99.0% 1:30,000
Prader-Willi syndrome 93.8% 1:25,500
KNOVA NIPT £950
ConditionDetectionPrevalence
Autosomal Trisomies
Trisomy 21 (Down Syndrome) >99.9% 1:800
Trisomy 18 (Edwards Syndrome) >99.9% 1:5,000
Trisomy 13 (Patau Syndrome) >99.9% 1:25,000
Trisomy 15 >99.9% <1:1,000,000
Trisomy 16 >99.9% N/A
Trisomy 22 >99.9% N/A
Sex Chromosome Aneuploidies
Turner Syndrome (45,X) >99.9% 1:2,000
Klinefelter Syndrome (47,XXY) >99.9% 1:800
Triple X Syndrome (47,XXX) >99.9% 1:1,000
Jacob's Syndrome (47,XYY) >99.9% 1:1,000
Microdeletion Syndromes
DiGeorge Syndrome >99.9% 1:4,000
1p36 Deletion Syndrome >99.9% 1:5,000
Wolf-Hirschhorn Syndrome >99.9% 1:35,000
Cri-du-Chat Syndrome >99.9% 1:30,000
Langer-Giedion Syndrome >99.9% <1:1,000,000
9p Deletion Syndrome >99.9% <1:1,000,000
Jacobsen Syndrome >99.9% 1:75,000
Angelman Syndrome >99.9% 1:15,000
Prader-Willi Syndrome >99.9% 1:22,500
Smith-Magenis Syndrome >99.9% 1:15,000
18p Deletion Syndrome >99.9% N/A
18q22q23 Deletion Syndrome >99.9% N/A
Monogenic Conditions
Noonan Syndrome >98% 1:1,000–2,500
Cornelia de Lange Syndrome 96.7% 1:10,000–30,000
Osteogenesis Imperfecta 95% 1:10,000–20,000
Stickler Syndrome 99% 1:7,500–9,000
Rett Syndrome 89.5% 1:10,000
Achondroplasia 98.2% 1:15,000–40,000
Crouzon/Pfeiffer Syndrome 99% 1:25,000
Cleidocranial Dysplasia 75.5% 1:100,000
CHARGE Syndrome 98% 1:8,500–12,000
Kabuki Syndrome 98.3% 1:32,000
Tuberous Sclerosis (TSC1) 94% 1–2:10,000
Tuberous Sclerosis (TSC2) 94% <1:1,000,000
Craniosynostosis (TWIST1) 50.3% 2–4:100,000
Craniosynostosis (EFNB1) 94% N/A
Craniosynostosis (ERF) 93.6% N/A
Craniosynostosis (TCF12) 93% N/A
Smith-Lemli-Opitz (CDKL5) 79% 1:50,000
Sotos Syndrome 43.7% 1:14,000
PrenatalSafe Complete Plus £1,490
ConditionDetectionPrevalence
Autosomal Trisomies
Trisomy 21 (Down Syndrome) 99.54% 1:700
Trisomy 18 (Edwards Syndrome) 100% 1:5,000
Trisomy 13 (Patau Syndrome) 100% 1:16,000
Sex Chromosome Aneuploidies
Turner Syndrome (45,X) 98.11% 1:2,500
Klinefelter Syndrome (47,XXY) 100% 1:650
Triple X Syndrome (47,XXX) 100% 1:1,000
Jacob's Syndrome (47,XYY) 100% 1:1,000
Rare Chromosomal Aneuploidies
All Other Autosomal Aneuploidies 99% Variable
Chromosomal Deletions and Duplications
Genome-wide CNVs 99% 1:1,000
Microdeletion Syndromes
DiGeorge Syndrome 83.33% 1:4,000
Cri-du-Chat Syndrome 83.33% 1:30,000
Prader-Willi Syndrome 83.33% 1:22,500
Angelman Syndrome 83.33% 1:15,000
1p36 Deletion Syndrome 83.33% 1:5,000
Wolf-Hirschhorn Syndrome 83.33% 1:35,000
Jacobsen Syndrome 83.33% 1:75,000
Langer-Giedion Syndrome 83.33% <1:1,000,000
Smith-Magenis Syndrome 83.33% 1:15,000
Inherited Monogenic Disorders
Noonan Syndrome (8 variants) N/A 4-10:10,000
De Novo Monogenic Disorders
Bohring-Opitz Syndrome N/A <1:1,000,000
Cardiofaciocutaneous Syndrome N/A 4-10:10,000
CHARGE Syndrome N/A 6-12:100,000
Osteogenesis Imperfecta N/A 5-7:100,000
Stickler Syndrome N/A 1:10,000
Crouzon/Pfeiffer Syndrome N/A 1-9:100,000
Achondroplasia N/A 1-2:10,000
Cornelia de Lange Syndrome N/A 1-10:100,000
Alagille Syndrome N/A 1-3.3:100,000
Rett Syndrome N/A 4-10:100,000
Cornelia de Lange Syndrome (Classic) N/A 1-10:100,000
Sotos Syndrome N/A 7-8:100,000
Schinzel-Giedion Syndrome N/A 1:>1,000,000
Holoprosencephaly N/A 1:16,000
Optional Features
Fetal Sex Determination 99.9% ~50%

Detection rate is the proportion of affected pregnancies the test correctly identifies. Figures come from each laboratory's validation studies and may not reflect the general population; your midwife will confirm the figures for the test you choose.

Our Pricing

Our Pricing

Transparent. Personalised. No surprises.

Aneuploidy NIPT From £295 Book
PrenatalSafe 3 UK From £325 Book
Panorama NIPT From £355 Book
Panorama Microdeletions From £525 Book
Niptify NIPT From £525 Book
Unity Complete Screen From £800 Book
KNOVA From £950 Book

20 Min Midwife
Counselling

Frequently Asked Questions

What’s the difference between basic and advanced NIPT?

Basic NIPT screens for the three most common chromosomal conditions: Down’s syndrome (Trisomy 21), Edwards’ syndrome (Trisomy 18), and Patau’s syndrome (Trisomy 13). Advanced NIPT includes everything in the basic test, but can also check for sex chromosome conditions, some rare genetic deletions (called microdeletions), and can tell you the biological sex of the baby if you choose to know. At Jeen, our genetic counsellors will help you decide which version is right for you during your consultation.

Is NIPT covered by the NHS?

At the moment, NIPT is only offered through the NHS in certain cases. For example, if you’ve had a high-risk result from a standard screening test. At Jeen, we offer private NIPT testing with flexible options, fast results, and full clinical support, including at-home appointments and expert guidance.

Can NIPT tell me the sex of my baby?

Yes, NIPT can usually identify the baby’s biological sex with high accuracy, but this is completely optional. If you’d like to know, just let your genetic counsellor know during your consultation and if you’d rather not find out, we’ll make sure it’s not included in your report.

Why do I need to send my scan before doing the NIPT?

We ask you to send us your pregnancy scan so our medical team can confirm that you’re at least 10 weeks pregnant and that the pregnancy appears to be developing as expected. This helps us check that NIPT is suitable for you and that your results will be as accurate as possible. It’s also important to know that NIPT screens for certain genetic conditions only. It doesn’t look for physical or structural differences, such as heart or organ development issues, which are usually identified later through ultrasound scans. By reviewing a recent scan (performed within one week of your blood draw), our doctors can make sure there are no early concerns before going ahead with your NIPT.

How long does it take to get results?

Your results will usually be ready within 2–10 working days from the time your sample arrives at our partner lab. The exact turnaround time depends on which NIPT you’ve chosen and the location of the laboratory. We’ll keep you informed throughout the process and arrange a follow-up consultation to talk you through your results as soon as they’re ready. Please note that delays can occur during public holidays in both the UK and the US. If your results indicate that follow-up testing is needed for your partner, we’ll act quickly to keep everything moving smoothly. Our priority is to get you the answers you need without unnecessary delays, so you can make confident, informed decisions for your pregnancy.

When can I take the NIPT and is it safe?

You can take the NIPT from 10 weeks into your pregnancy. Before booking your test with Jeen, we ask you to send us a recent pregnancy scan, such as a dating or viability scan, so our team of specialists can confirm you’re eligible to proceed. Yes, NIPT is completely safe for both you and your baby. It’s a non-invasive blood test that only requires a small sample from your arm, and there is no physical contact with the baby. This means there is no risk of miscarriage or harm to the pregnancy, unlike some invasive procedures.

How accurate is NIPT?

NIPT is over 99% accurate at detecting Down’s syndrome and also highly reliable for Edwards’ and Patau’s syndromes. It is more accurate than standard NHS screening and produces fewer false positive results, which means fewer people are sent for unnecessary follow-up testing.

Do I need midwife counselling before NIPT?

Yes. At Jeen, we believe everyone choosing NIPT should have the opportunity to speak with a qualified midwife beforehand. This conversation helps you understand what the test can and can’t tell you, and what your results may mean for you and your baby. It’s also a chance to ask questions and feel confident in your decision. If you would prefer to speak with a genetic counsellor, we can arrange this for an additional £30. Please note that choosing a genetic counsellor will also increase the total cost of your test by £30.

What happens if my NIPT result is high risk?

If your result shows a high risk for a condition, we’ll arrange a follow-up session with one of our genetic counsellors to explain exactly what it means. You’ll be given the option to have a diagnostic test, such as amniocentesis or CVS, which can confirm the result. We’ll support you at every step, with clear information and no pressure.

Will NIPT detect all possible conditions?

No, NIPT screens for a specific set of genetic conditions, mostly involving extra or missing chromosomes. It won’t detect all birth defects or structural anomalies, such as heart defects or limb differences. That’s why it’s important to still attend all your routine scans and check-ups during pregnancy.

References
  1. DiNonno et al. J Clin Med. 2019 Aug 26;8(9):1311.
  2. Martin et al. Genet in Med. 2023;25(8):100879.
  3. Nicolaides et al. Fetal Diagn Ther. 2014;35(3):212–7.
  4. Martin K et al. Genet in Med. 2023. doi.org/10.1016/j.gim.2023.100879
  5. Martin et al. Clin Genet. 2018 Feb;93(2):293–300.
  6. Dar et al. Am J Obstet Gynecol. 2022 Jan;227(1):79.e1–11.
  7. Kantor V, et al. Prenat Diagn. 2022 Jul;42(8):994–999.
  8. Dar et al. Am J Obstet Gynecol. 2022 Aug;227(2):259.e1–259.e14.
  9. Wapner et al. Am J Obstet Gynecol. 2015 Mar;212(3):332.e1–9.
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