Everyone carries genetic mutations that have the potential to cause a disorder—even if there is no family history of the disorder. And sometimes, these genetic mutations are passed on to their children.
If you’re pregnant or planning to become pregnant, Inheritest provides useful information about risks for certain genetic disorders and allows you to make informed decisions for a current or future pregnancy.
Inheritest is available in four different panels. Click on each of the panels below to view the specific disorders for which each panel screens.
Inheritest Comprehensive
Screens for more than 110 disorders, from the more common, such as cystic fibrosis, to the more rare, such as retinitis pigmentosa (also called RP).
Inheritest Society-Guided
Screens for 12 disorders included in the American College of Medical Genetics and Genomics and the American Congress of Obstetricians and Gynecologists guidelines.
Inheritest Ashkenazi Jewish
Screens for 39 disorders specific to individuals of Ashkenazi Jewish descent.
Inheritest Core
Screens only for cystic fibrosis, spinal muscular atrophy, and fragile X syndrome, some of the most common—and severe—genetic disorders.
Other testing options
In addition to carrier screening, we also offer: noninvasive prenatal testing (NIPT) and serum screening for Down syndrome and other conditions; diagnostic testing options for post-pregnancy or further confirmation of screening tests; and hereditary cancer screening.
