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What to do next

Genetic testing is the only way to find out if you carry an increased genetic risk of developing cancer.

Unlike other tests on the market, myRisk can help you and your doctor make medical decisions, and is covered by most health insurances.

Fill out the following form to create a prescription that you can take to your healthcare provider.

What to do next
THE FORM

Or Talk to a Doctor Today

If you don’t have a doctor, or would like to speak with one quickly, we have partnered with CareClix, a TeleHealth company. CareClix can take appointments over the phone or online. The cost is just $45 and can talk to you now or on your schedule, when and wherever works best for you.

SCHEDULE APPOINTMENT

Learn More about Genetic Testing

myRisk can be interpreted by your doctor to make medical decisions, and includes the riskScore Breast Cancer Prediction Tool* (clinically validated to predict a woman’s 5-year and remaining lifetime risk of developing breast cancer).

LEARN MORE

Want to learn more about your results?

Let us help guide you on what to do next. Click here to get more information from our Genetic Counseling Chatbot.

LET'S CHAT

Get a More Comprehensive Result

The Hereditary Cancer Quiz gives you a result immediately upon meeting a red flag; however you may have more than one red flag in your personal and family history. To best guide your conversation with your provider, you may want to fill out the Family History Tool. This application will provide you with a more comprehensive summary of your personal and family history of cancer.

For Your Provider

This application does not take into account several other red flags. Please ask your patient if any of the following applies to them:

  • Hereditary Breast and Ovarian Cancer syndrome:
    • A previously identified BRCA mutation
  • Lynch syndrome:
    • MSI High histology before age 60:
      • Mucinous
      • Signet ring
      • Tumor infiltrating lymphocytes
      • Crohn's-like lymphocytic reaction histology
      • Medullary growth pattern
    • A previously identified Lynch syndrome mutation

The above information is based on the family history provided by the patient, you may need to ask additional questions in order to get all the information needed to make an assessment.