Non-Invasive Prenatal Testing
A Simple Test. A Peaceful Pregnancy.
Non-Invasive Prenatal Testing
NIPT is a safe and accurate screening test that examines fetal DNA through a maternal blood sample. It assesses the risk for common chromosomal conditions such as Down syndrome and other trisomies. Non-invasive and highly reliable, NIPT gives expecting parents peace of mind and valuable insight into their baby’s genetic health—early in pregnancy.
What Does It Do?
NIPT is a screening test that analyzes fetal DNA in maternal blood to assess the risk of chromosomal conditions like Down syndrome, Edwards syndrome, and Patau syndrome.
Polygenic Risk Score (PRS)
PRS is not used; the test gives direct risk probabilities for trisomies and sex chromosome aneuploidies.
Who Benefits?
Pregnant women over age 35.
Women with abnormal ultrasound or serum screening.
Couples with previous pregnancy involving chromosomal abnormality.
Core Pillars
Non-Invasive
Safe for mother and baby.
Next-Gen Precision
High accuracy for trisomies
No Anxiety
Early detection for peace of mind.
MyDNA Gene Proactive
Fostering well-being by assessing and managing predisposition of traits, lifestyle diseases and chronic health conditions.
Free Consultation
Speak with our genetic counselors
Technical Specifications
| Specification | Value |
|---|---|
| Technique | Cell-free DNA (cfDNA) Analysis |
| Platform | NGS |
| Accuracy | 99% for Trisomy 21 |
| Sample Type | Maternal Blood (10+ weeks gestation) |
| Turnaround Time | 8–10 days |
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