What is Carrier Screening?

Carrier screening is a special type of genetic test that an individual can take to see whether they carry a genetic variant for a specific genetic disorder. Individuals usually are not impacted by the disorder themselves, but are interested in the chances of passing on the gene to a child. Carrier screening is commonly done before or during pregnancy and can help better inform individuals on the future health of their child.

Who can Benefit from Carrier Screening?

  • Couples considering trying for pregnancy or are already pregnant

  • Some of the genetic disorders that are commonly screened for are:

    • Cystic fibrosis

    • Hemoglobinopathies

    • Spinal muscular atrophy (SMA)

    • Fragile X Syndrome

    • Tay-Sachs Disease

How Can Clover Genetics Help?

  • We can provide risk assessments and assist in helping individuals or couples understand their likelihood of passing on a genetic condition to their future children

  • We can facilitate carrier screenings by request in coordination with an individual’s physician or facilitated through our team.