Our Approach

We focus on actionable genetic risks. Evidence based genetic risks that you, working with your physician, can do something about. We concentrate on the impact of genetics on medications and serious medical risk factors.

We enable you to partner with your physician - actionable information is provided to both you and your physician.

We frequently re-analyze your genetic data and your physician and you will be alerted if an important new issue is found.

We help you and your physician keep up with the latest medical knowledge about genetics. We revise our existing information based on the latest medical science, and also add to the medications and risks that we cover. Because we keep your genetic information on file, the new information will automatically be applied to your genetics.

Because we do not test for all possible variants and laboratory testing is not perfect, a negative result does not mean that there is no risk for a particular medical risk or a particular medication – gene interaction.

ActX is intended for informational and not diagnostic use. Since not all variants are checked for, high risk patients for serious risks should be tested using gene specific sequencing tests.

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College of American Pathologists