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Carrier Screening with Newlife IVF

Comprehensive carrier screening is an at-home genetic test that checks to see if you have a higher chance of having a baby with a serious inherited genetic disease. It tests for up to 343 genetic diseases that can affect children, including cystic fibrosis, spinal muscular atrophy, Tay-Sachs Disease, and fragile X syndrome.

For donor recipients who are Newlife IVF clients
Results in 4 - 6 weeks
Saliva tube icon
Buccal swab collection
Test is for
Free Shipping

2-day return shipping Australia wide

Fast Results

Results in 4-6 weeks

What's included

Frequently asked questions

From the moment we receive your saliva sample, the turnaround time to get your results are 4 to 6 weeks.

80% of babies born with an inherited genetic condition had no family history of it. That’s why Eugene’s carrier screening is relevant when you are planning a pregnancy, regardless of your family background or history.

This test is not meant to diagnose a person with any of the conditions screened for.

As a healthcare company, we comply with the most stringent local and international privacy and security regulations. We take incredible care to use technical, process and physical safeguards to secure your personal information and protect it against misuse, loss or alteration.

Finally, Eugene doesn’t share any of your data with anyone but you, the lab, Newlife IVFand (with your express permission) your doctor. To learn more about how our partner lab uses and stores your data, see the Fulgent privacy policy