About genetic testing

According to the U.S. National Library of Medicine, “Genetic testing is a type of medical test that identifies changes in chromosomes, genes, or proteins. The results of a genetic test can confirm or rule out a suspected genetic condition or help determine a person’s chance of developing or passing on a genetic disorder.”¹

It’s a process that typically involves a simple blood draw or saliva sample that is then analyzed to:

1. aid in family planning by determining carrier status for genetic disorders a parent(s) could pass on to children (known as carrier screening)
2. gain insights about the health of your baby during pregnancy through various tests, from serum screening to noninvasive prenatal testing (also called cfDNA screening) to diagnostic testing
3. assess your risk levels for specific hereditary cancers, such as breast, prostate, and pancreatic

• Examine the various types of genetic testing available
• Learn more about diseases and conditions that can be identified through genetic testing
• Watch our genetic counseling videos

Visit the billing section of our website or use our cost estimator.

Reference

1. U.S. National Library of Medicine. Genetics Home Reference. What is genetic testing? https://ghr.nlm.nih.gov/primer/testing/genetictesting. Accessed June 15, 2017.