Molecular Genetic Testing

Also known as: molecular diagnostics.

What is molecular genetic testing?

Molecular genetic testing refers to a wide variety of tests performed on blood and tissue to screen for genetic disorders. It can be performed on unborn babies or other people to determine if they are carriers of a particular disease. The test examines cells or strands of DNA to look for signs of a genetic disorder.

What happens during the procedure?

All that’s required for the test is a basic blood draw, typically from the arm but sometimes from another area of the body. Then the blood sample is taken to a laboratory for testing.

Is any special preparation needed?

No special preparation is needed for the test.

What are the risk factors?

There are slights risks of infection, bleeding, bruising or swelling related to the blood draw.


Reviewed by: Parul B Jayakar, MD

This page was last updated on: June 21, 2019 01:28 AM

Weekly Support Programs

Genes & Cocktails [POSTPONED]

This event has been postponed. Please join us for an intimate conversation on personalized medicine and preconception screening, with special speakers Vladi Yurovsky, Daria Salyakina, Phd, and Debbie Wasserman, MS. Come get screened for Jewish genetic diseases! Learn more.