Non-Invasive Prenatal Test (NIPT)
Pregnancy comes with many questions. EasyDNA’s Non-Invasive Prenatal Test (NIPT) gives you clear, clinically reliable answers early. Using just a small sample of the maternal blood, our advanced screening technology analyses your baby’s DNA to identify the risk of the most common chromosomal conditions, all without any invasive procedure and with zero risk to you or your baby.
This test screens for:
- Down Syndrome (Trisomy 21)
- Edwards Syndrome (Trisomy 18)
- Patau Syndrome (Trisomy 13)
Start your pregnancy with confidence. Order today and receive your results in as little as 5 to 7 working days.
What Is Non-Invasive Prenatal Test NIPT and How Does It Work?
Non-Invasive Prenatal Testing (NIPT) is a cutting-edge screening method that detects cell-free foetal DNA circulating naturally in the mother’s bloodstream during pregnancy. Using Next Generation Sequencing (NGS) combined with advanced bioinformatics analysis, EasyDNA’s NIPT can identify chromosomal irregularities with outstanding precision.
Because it requires only a maternal blood draw, NIPT is entirely non-invasive making it a much safer alternative to procedures like amniocentesis or CVS, which carry a small but real risk of miscarriage.
Non-Invasive Prenatal Testing (NIPT) is an advanced screening test that analyses cell-free foetal DNA found in the mother’s bloodstream, therefore there is no risk of miscarriage.
Which Conditions Does EasyDNA’s NIPT Screen For?
Not all prenatal screening tests are created equal. EasyDNA offers two carefully designed packages so you can choose the level of detail that’s right for you, whether you’re looking for core reassurance or the most comprehensive chromosomal overview available. Both packages are performed from a single blood sample, with no risk to you or your baby.
NIPT Basic for $575
Our NIPT Basic package is the ideal starting point for expectant parents who want reliable, early reassurance about the most common chromosomal conditions. It screens for the three trisomies most frequently identified during prenatal testing, giving you clinically significant information without unnecessary complexity.
- Trisomy 21 (Down Syndrome): caused by an additional copy of chromosome 21, associated with developmental differences and distinctive physical characteristics
- Trisomy 18 (Edwards Syndrome): an extra chromosome 18, often linked to serious medical complications
- Trisomy 13 (Patau Syndrome): a rare chromosomal condition involving an extra chromosome 13, affecting multiple organ systems
For many parents, screening for these three conditions provides exactly the peace of mind they’re looking for delivered quickly, safely, and at an accessible price point.
NIPT Plus for $635
For those who want a deeper level of insight, NIPT Plus takes screening significantly further. Building on everything included in the Basic package, NIPT Plus extends coverage to sex chromosome conditions and a broad range of microdeletion and microduplication syndromes, conditions that standard screening would simply miss.
Sex Chromosome Aneuploidies
Sex chromosome conditions occur when there is a missing or extra sex chromosome. NIPT Plus screens for four of these:
- Turner Syndrome (X0)
- Klinefelter Syndrome (XXY)
- Triple X Syndrome (XXX)
- XYY Syndrome
Key Microdeletion Syndromes
Microdeletion syndromes are caused by small missing segments of chromosomal material changes too subtle to be detected by standard chromosome analysis. NIPT Plus screens for some of the most clinically important of these, including:
- DiGeorge Syndrome
- Angelman Syndrome
- Prader-Willi Syndrome
- Cri du Chat Syndrome
- Wolf-Hirschhorn Syndrome
- 1p36 Deletion Syndrome
87 Additional Microdeletion & Microduplication Syndromes
Where NIPT Plus truly sets itself apart is in its extended coverage. Beyond the conditions listed above, the Plus package screens for a further 87 microdeletion and microduplication syndromes providing one of the most comprehensive non-invasive prenatal screening panels available. Examples of additionally screened conditions include:
- Smith-Magenis Syndrome
- Alagille Syndrome
- Langer-Giedion Syndrome
- 16p13.3 Microduplication Syndrome
- 1p32-p31 Deletion Syndrome
What Do Chromosomal Conditions Actually Mean for Your Baby?
Chromosomal abnormalities occur when a foetus inherits an extra or missing chromosome during cell division, a process known as aneuploidy. The impact varies significantly depending on which chromosome is affected.
- Down Syndrome (T21), for example, is compatible with life, and many individuals with the condition lead fulfilling lives, though developmental and physical challenges are common.
- Edwards Syndrome (T18) and Patau Syndrome (T13), on the other hand, are typically associated with far more severe medical complications, and sadly many affected pregnancies do not result in a live birth.
It’s also worth knowing that maternal age is one of the most significant risk factors. As a woman gets older, the likelihood of chromosomal non-disjunction, the error that causes these extra or missing chromosomes, increases. This is why NIPT is particularly recommended for women aged 35 and over, though it is a valuable option for expectant parents of any age who want early, reliable reassurance.
Is the Prenatal Screening Test NIPT Right For You?
EasyDNA’s prenatal screening test is recommended for:
- Women aged 35 and over
- Those who received a high-risk result from NHS combined screening
- IVF pregnancies
- Women with a personal or family history of chromosomal conditions
- Those with a history of miscarriage
- Anyone wanting early reassurance without undergoing invasive testing
Why Choose EasyDNA for Your NIPT?
We know that waiting for answers during pregnancy can be stressful. EasyDNA has been built around the belief that every parent deserves access to accurate, timely information delivered with care and clarity.
- Exceptional Accuracy: Our test achieves a detection rate of ≥99.9% for major trisomies, powered by Next Generation Sequencing and rigorous digitalised quality control.
- Completely Risk-Free: No needles near your baby, no invasive procedures just a routine blood draw from the mother’s arm.
- Early Availability: Testing opens from just 10 weeks of pregnancy, so you don’t have to wait.
- Fast Turnaround: Results are ready within 5-7 working days from the moment the lab receives your sample.
- Tailored Packages: Select the level of coverage that suits your needs, basic for core reassurance, or Plus for full comprehensive screening.
- Free Baby Gender Report: Find out whether you’re expecting a boy or a girl at no extra cost, if you choose to.
What’s Inside Your Prenatal Screening Test NIPT Kit?
Each kit is sent directly to your door and includes everything required for a smooth, straightforward experience:
- 2 x blood collection tubes for the mother’s sample
- Step-by-step instructions
- Consent forms
- Pre-paid return courier pouch for easy sample dispatch
Important: The blood sample must be collected by a qualified medical professional, your GP, a nurse, or a private practitioner. If you’d prefer a home visit from a trained nurse, EasyDNA can arrange this for you. An additional charge applies depending on your location. Contact our team for a personalised quote.
Once collected, simply seal your samples in the pre-paid pouch and send them back to our laboratory, it really is that simple.
Your NIPT Journey: Step by Step
- Order your test: select NIPT Basic or Plus and complete your order online
- Collect your sample: a qualified professional performs a simple blood draw (2 × 10ml tubes)
- Return to the lab: use the prepaid courier pouch to send your sample
- Laboratory analysis: foetal DNA is extracted and sequenced using advanced NGS technology
- Bioinformatics processing: sophisticated algorithms assess chromosomal data
- Receive your results: a clear, confidential report delivered within 5-7 working days
NIPT is a highly accurate screening tool, not a definitive diagnosis. A high-risk result means the probability of a chromosomal condition is elevated, but it does not confirm a diagnosis on its own.
If your results indicate elevated risk, we strongly encourage you to speak with your GP, midwife, or a specialist healthcare provider. They can advise on confirmatory diagnostic options such as amniocentesis or chorionic villus sampling (CVS).
Understanding Your Results: An Important Note
EasyDNA’s NIPT is one of the most accurate prenatal screening tools available, but it’s important to understand what your results do and don’t tell you.
NIPT is a screening test, not a diagnostic one. What this means in practice is that your results reflect a statistical likelihood, not a confirmed diagnosis. A high-risk result indicates an elevated probability that a chromosomal condition may be present, but it is not conclusive on its own and a low-risk result, while highly reassuring, is not a guarantee.
If your results come back as high risk, please don’t panic. The next step is simply a conversation with a medical professional. Your GP, midwife, or an obstetric specialist will be able to review your results in context, answer your questions, and walk you through any further testing that may be appropriate such as amniocentesis or chorionic villus sampling (CVS), both of which can provide a definitive diagnosis.
You don’t have to navigate this alone. Our team is also on hand to help you understand your report and point you in the right direction, should you need support before your medical appointment.
NIPT Premium Package for $1995
Looking for the most comprehensive prenatal screening available? Combine our most popular tests into one seamless experience:
- NIPT Plus: full chromosomal screening
- Non-Invasive Prenatal Paternity Test: confirm paternity without risk
- Baby Gender Test: find out the gender of your baby, this is optional and included at no extra cost.
All from a single blood sample and available from 10 weeks of pregnancy only.
Ready to Get Started? Order Your NIPT Today
Every parent deserves to feel informed and confident during their pregnancy. EasyDNA’s NIPT gives you clinically trusted answers early, without the wait, without the worry, and without any risk to you or your baby.
- A detection rate of ≥99.9% for the most common chromosomal conditions
- Results back in as little as 5-7 working days
- A completely non-invasive process just a simple blood draw
- Clear, easy-to-understand reporting with expert support available every step of the way
Whether you’re seeking straightforward peace of mind or a comprehensive chromosomal overview with our Plus package, EasyDNA makes it simple to take control of your prenatal journey from as early as 10 weeks.
Don’t leave important questions unanswered. Order today and give yourself the clarity you deserve.
Explore More Prenatal Tests from EasyDNA
At EasyDNA, we offer a full range of prenatal testing, because every parent deserves clarity, confidence, and peace of mind from the very start.
Need to confirm paternity before your baby arrives? Our Non-Invasive Prenatal Paternity Test can be performed from as early as week 7 of pregnancy, with no risk to the mother or baby.
Curious about the sex of your baby? Our early Baby Gender DNA Test is 99.5% accurate and can be taken from week 7. Results arrive in just 7 working days, with a 4-working-day express option also available.
Frequently Asked Questions about the NIPT
Is NIPT the same as a diagnostic test?
No. NIPT is a prenatal screening test, not a diagnostic procedure. It calculates the statistical likelihood of chromosomal conditions based on foetal DNA analysis. Any high-risk results should be followed up with confirmatory diagnostic testing through your healthcare provider.
How early in pregnancy can I take the test?
From 10 weeks of pregnancy. This is the point at which sufficient foetal DNA is present in the maternal bloodstream to ensure reliable results. For twin pregnancies, samples must be taken from 12 weeks.
Is the test safe?
Completely. EasyDNA’s NIPT involves only a standard blood draw from the mother and carries no risk of miscarriage or harm to the baby.
How long will I wait for results?
In most cases, you’ll receive your report within 5-7 working days of the laboratory receiving your sample.
How accurate is EasyDNA’s NIPT?
The test detects major trisomies with a sensitivity of ≥99.9%, achieved through Next Generation Sequencing and validated bioinformatics pipelines.
What type of sample is required?
A standard maternal blood draw from the arm. No other sample is needed.
Can I find out my baby’s sex?
Yes, gender determination is included at no additional cost, based on the presence or absence of Y chromosome material in the maternal blood sample.
Does maternal age affect my results?
Maternal age influences the baseline risk of chromosomal conditions. Older mothers have a statistically higher likelihood of foetal aneuploidy due to nondisjunction events one reason NIPT is particularly recommended for women over 35.
Does NIPT screen for all genetic conditions?
No. NIPT focuses on chromosomal abnormalities detectable through cell-free DNA analysis and does not cover conditions caused by single-gene mutations, such as cystic fibrosis, unless these are part of a separate test panel.
What can affect the test’s accuracy?
The foetal fraction the proportion of foetal DNA in the maternal blood can be influenced by factors including early gestational age, high maternal BMI, certain medications, and IVF pregnancies. Our laboratory team will notify you if a retest is required.
Can I take the test if I’m carrying twins?
Yes. Twin pregnancies are eligible, but blood samples must be collected from 12 weeks of pregnancy rather than 10.
What’s the difference between NIPT Basic and NIPT Plus?
NIPT Basic covers the three major trisomies (T21, T18, T13). NIPT Plus extends this to include four sex chromosome aneuploidies and 93 microdeletion and microduplication syndromes offering a far broader level of reassurance.
What should I do if I get a high-risk result?
Contact your GP, midwife, or healthcare provider as soon as possible. They will review your results and may recommend diagnostic confirmation via amniocentesis or CVS. Remember a high-risk NIPT result is not a diagnosis, and further testing is available to provide certainty.