Accuracy rates depends on the chromosome.

The NIPT test examines cell-free DNA (cfDNA) released from the placenta into the mother’s bloodstream. The NIPT test detects chromosomal abnormalities within this fetal cfDNA present in the mother’s blood, with a simple blood draw.

A NIPT test is a screening test — not a diagnostic test. This means that it can’t diagnose a genetic condition with certainty. It can, however, predict whether the risk of a genetic condition is high or low. Therefore, you need to have the results read by a professional. We strongly recommend you to take the results to your OBGYN to interpret the results.

Any pregnant women could get a NIPT test but it is especially recommended for pregnant women:

– aged over 35 years old

– who have a personal/family history of chromosomal disorder (or from the baby’s father)

Yes, our package includes the option of having fetal sex reported.

NIPT test is performed by collecting blood sample which poses no threat to fetus.

The blood sample will be sent GC Genome, a leading clinical genomic laboratory in South Korea. Our laboratory service accredited by the College of American Pathologists (CAP) from the USA which is the largest association to provide a laboratory accreditation and is a gold standard in laboratory quality assurance.

Our nurse practitioner will come to your preferred place and collect the blood sample.

We recommend you to talk to your doctor for next course of action that may include further testing.