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CLINICAL GENETICS

NIPT Standard – Non-Invasive Prenatal Test Standard

A Safer Way to Learn About Your Baby’s Health.

From 10 weeks of pregnancy, NIPT Standard screens for Down syndrome, Edwards syndrome, and Patau syndrome, while also providing accurate gender determination. And it doesn’t stop there — the test further checks for sex chromosome aneuploidies and additional autosomal aneuploidies. All of this is done through a simple, safe blood draw from the mother, with no risk to the baby.

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What is NIPT Standard?

NIPT Standard is a more comprehensive version of the Non‑Invasive Prenatal Test, designed for parents who want deeper insights into their baby’s chromosomal health.

From as early as 10 weeks of pregnancy, NIPT Standard provides:

  • Screening for Trisomy 21 (Down syndrome)
  • Screening for Trisomy 18 (Edwards syndrome)
  • Screening for Trisomy 13 (Patau syndrome)
  • Detection of 6 Sex Chromosome Aneuploidies (SCAs):
    • Turner syndrome (XO)
    • Triple X (XXX)
    • XYY
    • Mosaic variations (XO+XY, XXX+XY)
  • Screening for 19 additional autosomal aneuploidies
  • Accurate sex identification
  • Fetal fraction estimation (measuring the proportion of fetal DNA in the mother’s blood to ensure test reliability)

 

All of this is achieved through a simple, safe blood draw from the mother, with no risk to the baby.

This test is designed for:

  • Expectant parents wanting early reassurance
  • Families with history of chromosomal conditions
  • Parents seeking a safe alternative to amniocentesis or CVS
  • Parents wanting a comprehensive view of their baby’s chromosomal health

Why This Test Matters

For Patients & Families

  • Identify inherited cancer risks early.

  • Take preventive steps such as enhanced screening or lifestyle changes.

  • Share results with relatives for family‑wide health planning.

For Providers

  • Improve patient care with genetic insights.

  • Guide referrals, screening protocols, and preventive interventions.

  • Support cascade testing for at‑risk family members.

For Proactive Consumers

  • Even without a family history, you may carry mutations that increase cancer risk.

  • Knowledge empowers you to take control of your health.

Conditions screened

Trisomy 21 (Down syndrome)

Trisomy 18 (Edwards syndrome)

Trisomy 13 (Patau syndrome)

6 Sex chromosome

Aneuploidies (SCAs) (XO/XXX/XYY/XO+XY/XXX+XY)

Other 19 autosomal

Aneuploidies

Sex identification

Fetal fraction estimation

Endocrine Tumors

RET (MEN2), VHL, SDHx genes, PTEN

Other Cancers

Li‑Fraumeni syndrome (TP53)

Kidney cancers (FH, FLCN, VHL)

Brain tumors and sarcomas

What you will learn from this test

  • Early risk assessment for trisomies
  • Early risk assessment for all chromosomal aneuploidies
  • Whether further testing is needed weeks before ultrasound scans
  • Your baby’s gender with high accuracy
  • Whether more invasive testing or specialist care may be needed
  • Fetal fraction percentage confirming reliability
  • Knowledge to plan ahead with confidence

Why choose NIPT?

  • Early detection : from 10 weeks
  • Non-invasive: just a maternal blood draw
  • Highly accurate: >99% for trisomies and aneuploidies
  • Fetal fraction included for quality assurance
  • Validated in African populations

How it works

Order the test online or through your provider

Provide one blood draw from the mother’s arm

Receive results within 5–7 days

Pricing

Plan with the right information.
Order Your NIPT Standard  Today

NIPT – Non-Invasive Prenatal Test

₦475,000

(For Provider)

Order Test

NIPT – Non-Invasive Prenatal Test

₦500,000

(Direct-to-Consumer)

Order Test