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About genetic testing

What is 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

Want to learn more?

Questions about costs and insurance coverage?

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

If you’ve not had a test and have questions about costs or coverage, use our estimator.

If you have already had a test performed, we can help answer questions about results.

Ask questions about genetic testing options or results, or schedule an appointment.

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.