Guide

What is NIPT?

NIPT (non-invasive prenatal testing) is a blood test you can have from 10 weeks of pregnancy. It looks at small fragments of your baby’s DNA in your blood to screen for chromosomal conditions such as Down’s syndrome.

  • From 10 weeks
  • No risk to baby
  • Results in about 5 working days
  • No GP referral

How NIPT works

During pregnancy, small fragments of DNA from the placenta circulate in your blood. These closely reflect your baby’s DNA. The test counts these fragments to see whether there is extra or missing chromosome material.

What it screens for

All our NIPT tests screen for Down’s (trisomy 21), Edwards’ (trisomy 18) and Patau’s (trisomy 13) syndromes and sex chromosome conditions. Advance and Absolute add microdeletions. You can also choose to find out your baby’s sex.

Is it safe?

Yes. It’s a simple blood test from your arm, so there’s no risk to your baby or your pregnancy, unlike diagnostic tests such as CVS or amniocentesis.

Screening, not diagnosis

NIPT tells you whether there is a lower or higher chance of a condition. A higher-chance result needs to be confirmed with a diagnostic test before any decisions are made.

Our NIPT tests

What’s screenedMost chosenStandard£295 Advance£345Widest screenAbsolute£425
Down’s syndrome (trisomy 21)✓✓✓
Edwards’ syndrome (trisomy 18)✓✓✓
Patau’s syndrome (trisomy 13)✓✓✓
Sex chromosome conditions: Turner, Klinefelter, Jacobs (XYY) and Triple X✓✓✓
Baby’s sex (optional)✓✓✓
6 common microdeletions–✓✓
92 microdeletions––✓
Results in about 5 working daysBookBookBook
Please note: this guide is general information. NIPT is a screening test and doesn’t replace advice from your midwife or doctor.

More guides

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From £295. A 15-minute visit at our Croydon clinic, with no GP referral.

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