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What is pharmacogenetics (PGx)?

Pharmacogenomics is the study of how inheritable genetic differences in individuals can affect how they react to medications and treatments. Every person is different and may metabolize, absorb, and respond to treatments in individual ways that are determined by their DNA.

PGx is meant to be a tool for doctors to reference in treating patients that allows them to have an idea as to how a patient may metabolize, absorb, and respond to particular treatments. The goal is to reduce trial and error and improve patient care overall.

What can the OmniPGx test do for me?

An OmniPGx test kit will help your doctor determine whether you are at greater risk for side effects or if you may benefit more or less from a particular medication. Your doctor will find the right treatment for you much faster than the traditional “trial & error” methods of diagnosis and treatment.

How does the OmniPGx test work?

After you purchase an OmniPGx test, you will receive a DNA sample collection kit in the mail within 1-2 business days of your purchase.

First you must activate your kit online by using the kit number that comes with your PGx kit. Activation is required before your sample can be processed in the OmniPGx lab. After you complete this step, you can begin DNA collection.

Within the kit you will find step-by-step instructions on how to collect your DNA sample via a simple cheek swab. Once you complete your DNA collection, place the sample back in the box and drop the box in the mail. Your kit will automatically be shipped to the OmniPGx testing laboratory, and we'll take it from there.

After shipping your kit, all you need to do is wait for your results to be ready. This typically takes around 5-7 business days after the OmniPGx lab receives your sample.

Once your results are ready, you can unlock them by booking a free 30-minute phone consultation with a board-certified OmniPGx healthcare provider. After booking, you can access your results.

What information will the test provide?

The OmniPGx test panel contains actionable information on 322 different drugs and over 60 genes. The provided information includes potential risk for certain diseases, how quickly your body will metabolize certain medications, and potential drug-gene interaction risks.

Who may benefit the most from an OmniPGx test?

Any patient who is set to begin treatment with one of the 322 medications covered in our panel is likely to benefit from taking the test. Additionally, the test may be beneficial to patients who have struggled to achieve desired results from multiple “trial and error” attempts at treatment for various health conditions. These are the perfect candidates for an OmniPGx test, however, the test can also be beneficial to patients who fall outside of these categories.

What is the cost of the test and how do I purchase one?

The cost for a test plus the services provided by a board-certified OmniPGx healthcare provider is $499. The provider services include an in-depth consultation to review your test results as well as answering any additional questions you may have. Insurance billing is not available. You can purchase an OmniPGx test online through our website at omnipgx.com/purchase. OmniPGx accepts payment through all major credit cards, health savings accounts (HSAs), and Paypal.

What is the difference between the OmniPGx test and other genetic tests?

The OmniPGx test differs from other genetic tests in two major ways. First, it is a pharmacogenetic test, meaning its primary focus is on how your genes may cause you to respond to different medications. Unlike other genetic tests, the OmniPGx test does not provide results for ancestry, cosmetic traits, or similar information found in other existing genetic tests. Second, the OmniPGx test is one of the first scientifically validated tests of its kind. It is designed under high-level scientific and clinical standards to assist your healthcare provider in optimizing selection of the right medication for you. Although the primary purpose of the OmniPGx test is not to diagnose disease risk or any hereditary diseases, you may receive these incidental findings in your genetic results. You may wish to discuss these secondary findings with your primary healthcare provider upon viewing your results.

How long will it take to see my results?

You will be able to access your results within 3-4 weeks from the time our lab receives your DNA sample. Your results will be viewable (and printable) on your OmniPGx account, which is a secure, easy-to-use online portal. You create your OmniPGx account when you first receive your test kit in the mail.

What can I do with my results?

After your consultation with our medical provider, you will have complete access to your test results. We encourage you to share your results with your doctor. Keep in mind, you should not make any changes to medications you are taking without first consulting the appropriate healthcare provider.

Will insurance cover my OmniPGx test?

When ordered by your doctor, some insurance plans within the U.S. may contribute to the cost of the test.

Note: Insurance billing is not available for tests purchased online.