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Gender Testing
Gender Testing
SneakPeek® Clinical Early Gender DNA Test
Boy orGirl? Know sooner than ever before. The only 99.9% accurate early gender DNA test, starting at 6 weeks into pregnancy. Results emailed straight to you the next day!*
SneakPeek Clinical by Gateway Genomics is the only clinically proven early gender DNA test that lets you discover your baby’s gender months ahead of schedule, so you can prepare for your little one and share with family and friends! The test uses non-invasive prenatal testing (NIPT) to look for male Y chromosomes from a small sample of your blood. If male Y chromosomes are found, that means baby is a boy. If none are found, baby is a girl. SneakPeek is the leading provider and most accurate early gender DNA test on the market, trusted by over 500,000 moms and practitioners.
Learn more:
https://sneakpeektest.com/early-clinical-baby-gender-blood-test/
https://sneakpeektest.com/test-eligibility-calculator/
https://sneakpeektest.com/gender-dna-science/
*Subject to postal delays
SneakPeek® early gender testing can be done independently or added on to any package listed on the Services page for $109.
Genetic & Carrier Screening
Genetic & Carrier Screening
Panorama™ is a blood-based genetic, prenatal screening test of the pregnant person that screens for common chromosomal conditions that affect a baby’s health. Panorama™ uses SNP*-based technology to deliver highly accurate results and unique insights for both singleton and twin pregnancies.
Panorama™ can be performed as early as nine weeks gestation. Most results will be returned to your clinician within 5-7 calendar days from the date that samples are received.
Panorama™ is a screening test, which means that this test does not make a final diagnosis. A high risk result means that your pregnancy has a higher chance of having a specific genetic condition. However, you cannot know for sure if your baby has that condition based upon the screening result alone. All medical decisions should be made after discussion with your healthcare provider regarding diagnostic testing during the pregnancy, like chorionic villus sampling (CVS) or amniocentesis, or testing the baby after birth.
Learn more about this specific test here: https://www.natera.com/womens-health/panorama-nipt-prenatal-screening/
*SNP, single nucleotide polymorphism
Horizon™ genetic carrier screening helps couples determine the risk of passing on serious genetic conditions to their child. Carrier screening can be performed either before or during pregnancy. All of us are carriers of at least one genetic condition. Most carriers are healthy with no family history, but they are at risk of passing on a genetic condition to their child. Carrier screening is a genetic test that identifies if you carry a gene with a change, or variant, that can impact your child. When performed before conceiving, genetic carrier screening can provide actionable knowledge and the opportunity to pursue alternative reproductive options. Carrier screening during pregnancy can help couples decide on prenatal or infant diagnostic testing, and if necessary, help them prepare emotionally, medically, and financially for a baby affected by a genetic condition.
Learn more about this specific test here: https://www.natera.com/womens-health/horizon-advanced-carrier-screening/
Panorama™ testing can be run through your insurance with the maximum cash pay price of $250
Panorama™ + Horizon™ screening can be run through your insurance with a maximum cash pay price of $350
*each test includes Fetal Sex and Rh type
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