Genetic Testing

Overview

Genetic testing examines an individual's DNA to identify variations that may be linked to certain conditions or traits. Such testing requires a sample of blood, hair, skin, tissue, or amniotic fluid. The results inform care, diagnoses, and family planning.

Genetic testing can confirm a suspected diagnosis or inform prospective parents about their child's disease risks based on changes in the genes or chromosomes of their fetus. It can help determine how often people should be screened for cancer or how to attack a specific tumor. It can also detect whether someone is a carrier of an autosomal recessive condition, such as sickle cell disease. Genetic testing can even examine how a person's individual genes may influence how they process medications, a field called pharmacogenetics.

In recent years, polygenic risk scores for embryos have become a novel and controversial offering. These genetic estimates quantify the risk of developing traits determined by multiple genes—like high cholesterol or diabetes—and guide decisions about which embryo to implant during in vitro fertilization. The scores remain legal in the US, though they have been banned elsewhere, including in the UK. The first US embryo selected in this manner was born in May 2020.

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