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Pharmacogenomic (PGx) Tests

What is PGx testing?

  • Pharmacogenomic (PGx) testing is a once in a lifetime genetic test that identifies how your body processes medications

  • Our comprehensive test looks at 45 key genes that impact medication use, including CYP1A2,CYP2C9, CYP2C19, CYP2D6, CYP3A4, MTHFR, and TPMT


Why get PGx testing?

  • Ensure you are taking the right medications

  • Genetic variations can affect medication safety and effectiveness

  • Customizing your therapy based on your results can prevent dangerous side effects, avoid ineffective medications and improve health outcomes


What does it include?

  • A report of your genetic results and personalized recommendations for your medications based on the most up-to-date evidence

  • You'll also learn how your body processes hundreds of other medications


PGx testing can benefit many people, including those with:

  • Chronic health conditions

  • Multiple medications

  • Past medication side effects

  • Condition not responding to medication

  • Future treatment decisions

Medication recommendations based on clinical guidance from the Clinical Pharmacogenetics Implementation Consortium (CPIC) and the Federal Drug Administration (FDA).

Common Medications and Health Conditions Impacted by Genetics


Our lab partners are CLIA-certified and CAP accredited.

Pharmacogenomic and nutrigenomic test results are not meant to diagnose, cure or treat a disease. Medication or treatment should not be changed without consulting with your healthcare provider.

Dr. Yandell creates evidence-based recommendations for your medication therapy and nutrition based on your results and medication or health history. These recommendations can be shared with your healthcare provider to determine the best treatment for you.

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