Frequently asked questions
The things people ask before they test.
General
What does this test screen for?
Inherited risks linked to cancer, heart conditions, cholesterol disorders and other medically actionable conditions: 180+ clinically validated genes across cancer (65+), cardiovascular (85+) and additional health risks (25+).
Who is this test right for?
Adults who want to understand inherited health risk early, whether or not they have a family history. A genetic counselor and physician review every result, so you are not left to interpret it alone.
How is the testing done?
You collect a simple saliva sample at home and return it in the prepaid mailer. It's analyzed at a CLIA-certified, CAP-accredited laboratory.
Results & actions
What will my results tell me?
Whether you carry a pathogenic or likely pathogenic variant in one of the genes on the panel, and what that means for your care. We only report findings a doctor can act on.
Does a positive result mean I'll develop the condition?
No. A finding means you carry an inherited risk, not a diagnosis. It tells you and your doctor where to look earlier and act sooner.
What does it mean if no genetic variants are found?
It is important to know that this is a proactive genetic screen. It focuses on the most well known and actionable genetic changes known to be associated with heritable forms of cancer and heart disease.
No test can exclude all risks.
If you have a strong personal or family history of disease, this test may not be right for you. Please speak to our genetic counselors if you require further support.
What actions can I take with my results?
Depending on the finding: earlier or more frequent screening, preventive medication, targeted lifestyle changes, and where relevant a referral to the right specialist. Your action plan is personalized.
Is genetic counseling included?
For an actionable result, yes: a one-on-one session with a genetic counselor who explains what it means and what to do next. If nothing actionable is found, your report explains the outcome in plain language, so you're never handed raw data and left on your own.
Testing process
How accurate is this test?
Samples are processed at a CLIA-certified, CAP-accredited lab, meeting national standards for clinical testing, and results are reviewed by a genetic counselor and physician before they reach you.
How long do results take?
Typically around 4 to 6 weeks from when the lab receives your sample.
Privacy & insurance
How is my genetic data protected?
Your data is handled under strict security controls (SOC 2 Type I & II). It is never sold, and you control who can see your results.
Will this affect my insurance or employment?
Under GINA (the Genetic Information Nondiscrimination Act), US health insurers and employers cannot use your genetic information against you. Important: GINA does not cover life, disability or long-term care insurance.