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Hercheck Nipt All Chromosomes

  • Report in 10 Day
  • No fasting needed
  • Home collection
  • 5 parameters

What the Hercheck Nipt All Chromosomes checks

  • HerCheck NIPT All Chromosomes is a non-invasive prenatal screening test. This method involves the analysis of cell-free fetal DNA (cffDNA) circulating in maternal blood
  • without any risk to the fetus
  • to screen for aneuploidies (extra/missing chromosomes) across all 23 pairs
  • not just the common trisomies (21, 18, 13). It provides comprehensive insights into fetal health
  • covering rare autosomal trisomies and sex chromosome abnormalities.

How to prepare

No fasting is needed. Drink water as usual and tell the phlebotomist about any medicines you take.

Unsure about your report values? Use our report checker — and always discuss results with your doctor.

Hercheck Nipt All Chromosomes – FAQs

What is the price of Hercheck Nipt All Chromosomes?

The Hercheck Nipt All Chromosomes costs ₹12,500 (MRP ₹20,000, you save 38%) with home sample collection. Home collection charges, if any, are shown before you confirm the booking.

Is fasting required for Hercheck Nipt All Chromosomes?

No fasting is needed for this test. You can give the sample at any time of the day.

When will I get the Hercheck Nipt All Chromosomes report?

The report usually comes in 10 Day after the sample reaches the lab. It is sent on WhatsApp and email.

Can I give the sample for Hercheck Nipt All Chromosomes at home?

Yes. A trained phlebotomist visits your home with a sealed kit at the slot you choose. Enter your pincode while booking to check home collection in your area.

What does the Hercheck Nipt All Chromosomes include?

It checks 5 parameters: HerCheck NIPT All Chromosomes is a non-invasive prenatal screening test. This method involves the analysis of cell-free fetal DNA (cffDNA) circulating in maternal blood, without any risk to the fetus, to screen for aneuploidies (extra/missing chromosomes) across all 23 pairs, not just the common trisomies (21, 18, 13). It provides comprehensive insights into fetal health, covering rare autosomal trisomies and sex chromosome abnormalities..

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