Your DNA is your baseline.
Test your baseline once, and every health choice you make after gets sharper.
180+
genes to start
across cancer, heart & additional risk, with more reports to come
One test to uncover what’s in your genes.
Sequence your DNA once, then build personalized action plans for the risks you were born with.
The earlier you see it, the more you can do.
Most inherited risks stay silent until something happens. Seeing them early is what makes prevention possible.
1 in 2
women with a BRCA1 or BRCA2 mutation will develop breast cancer by age 70, compared with about 1 in 14 in the general population.
CDC
1 in 17
people with heart disease carry the familial hypercholesterolemia gene variant, about 18 times more common than in the general population.
CDC Genomics and Precision Health
~1 in 50
healthy adults screened at a major US health system were found to carry a pathogenic variant for a hereditary cancer or heart condition.
Mayo Clinic Tapestry Study
7 in 8
people found to carry a hereditary cancer or heart disease risk variant had no prior diagnosis based on personal or family history alone.
Geisinger MyCode
7 in 10
people who learned they carried a hereditary risk went on to complete a recommended screening or procedure they had not had before.
Geisinger MyCode
Reproductive
Coming soon
Brain health
Coming soon
Drug response
Coming soon
Nutrition
Coming soon
Longevity
Coming soon
How it works
-
Activate your profile
Complete your profile, so your results are personalized to your health history.
- Add your health and family history
- Consent to testing in a few taps
- About ten minutes to complete
-
Provide your sample
One saliva sample, taken at home.
- Ships straight to your door
- At-home saliva sample, no blood draw
-
Accredited lab analysis
Your sample is analyzed by a CLIA-certified, CAP-accredited lab.
- CLIA/CAP-certified laboratory
- Medical grade analysis of 180+ genes
- Results in 4 to 6 weeks
-
Insights you can act on
Your results are broken down per health category in easy to understand language.
- Actionable insights, not raw data
- Guided by a genetic counselor
-
New reports over time
As new reports launch, unlock them from the sequence you already have.
- Your sequence stays securely stored
- Every report in one place
Sequence once. Guidance for life.
One sequence is all it takes. Your first report covers cancer and heart risk, and every future report interprets the same sequence.
-
Eugene Sequence$499
The one-time DNA sequence behind every report.
-
Annual membership
$100/yrFree first yearKeeps your sequence stored securely and your reports in one place.
-
Preventative health report$300
Your cancer and heart baseline: 180+ genes, with genetic counselor and physician review and a personal action plan.
$1,117.55$1,257.42
The highest standard for genetic testing.
Eugene works with CLIA-certified, CAP-accredited laboratory partners, chosen for accuracy and clinical rigor. Every order is reviewed by a genetic counselor.
185
genes on your first report
45,000
members served
What our community is saying
“One easy test gave me something I’d never had before: clarity. I discovered what health risks my genes might predispose me to, and what I could do to prevent them.”
“I didn’t want to wait until something went wrong. I wanted to act early. They explained what I could do to reduce my risks and helped me create a preventative care plan I could take straight to my GP.”
Matthew had no idea he carried a variant linked to Long QT Syndrome - a heart condition with no warning signs until a cardiac event. Eugene caught it early. Now he knows which medications to avoid and how to manage his risk before anything happened.
Are you a clinic or provider?
Offer Eugene to your patients or members. Concierge medicine and longevity clinics welcome.
About the test
How does membership work?
Sequencing is one-time. Membership is $100 a year: it keeps your genome securely stored, so new reports can be added anytime.
What does it screen for?
Inherited risk across cancer, heart and additional genes.
Results & support
Will I understand my results?
Yes. Every result is explained in plain language in the app. If we find something actionable, a one-on-one session with a genetic counselor is included to talk it through.