Pharmacogenetic Testing Frequently Asked Questions

Pharmacogenetic testing analyzes your DNA to predict how you will break down (metabolize) and respond to specific medications. This helps healthcare providers choose the most effective and safe medications and doses for you.

The test involves collecting a DNA sample through a cheek swab or blood draw. The sample is then analyzed to identify genetic variants that affect drug metabolism and response.

Anyone who is experiencing adverse reactions to medications or who has a family history of drug sensitivities may benefit from pharmacogenetic testing. It is especially useful for individuals on multiple medications or those with chronic conditions.

Results are generally available within two weeks for panel testing (non-cancer patients) and four weeks for sequencing (cancer patients). 

Coverage varies by insurance plan. Contact your insurance provider to find out if pharmacogenetic testing is covered. If not, Children's Mercy offers financial assistance and payment plans to help offset the cost.

If your insurance denies coverage, contact our Financial Counselor at (816) 234-3567 to apply for one-time financial assistance. Alternatively, you may choose to pay out of pocket or set up a payment plan.

The cost of testing varies. For those paying out of pocket, the cost of the panel test is currently  about $400. Children's Mercy also offers payment plans with an initial deposit of 20% and up to 24 monthly payments. 

Pharmacogenetic testing can help avoid adverse drug reactions, determine the most effective medications and dosages, and improve overall treatment outcomes by personalizing your medication regimen.

The testing process itself is safe and non-invasive. The primary risk is related to the privacy and security of genetic information, which is strictly protected by Children's Mercy.

To get started, schedule an appointment with the GOLDILOKs® Clinic to discuss medications and whether pharmacogenetic testing is right for you. Contact them at (816) 601-3360.