Trusted by teams at
Get your genetic baseline to use alongside labs, wearables, and lifestyle data to prioritize the actions that matter most.
Early access pricing: $49
Genetics in context
Start with your genetic baseline, then layer in periodic labs, daily wearables, and evolving lifestyle habits to build more personalized health insights.
WEARABLES & VITALS
(Daily)
LABS & BIOMARKERS
(Periodic)
GENETIC BASELINE
(Stable Foundation)
Trusted by teams at
Simple Process
From order to insights in three easy steps. Everything is handled for you.
Step 1
We ship a buccal (cheek) swab collection kit directly to your door. No blood draw needed.
Step 2
Provide your saliva sample and mail it back with the prepaid return label. That's it.
Step 3
Receive your personalized results and download your complete raw sequencing data.
What you'll learn
Start with 9 DNA-based health insights across core health areas. Ancestry is included too, as an added benefit.
This is just the start: more insights and traits are coming soon.
Your DNA baseline becomes even more useful when paired with labs, wearables, and the health data you already track.
Built for action
Personalized PRS report across key health traits
At-a-glance summary of High risk vs Not high risk results
Recommended next steps for each result
About this trait, technical details, and references for added context
Informational only; reflects relative genetic risk compared to a reference population and is intended as a starting point for conversations with your healthcare provider.
Example report
Privacy
Download your raw data anytime. Your genetic data is stored securely, with clear privacy practices you can understand.
Raw data download anytime
Private and secure data handling
Clear privacy practices
Pricing
$49
The Difference
Most consumer tests use microarray chips that read only a tiny fraction of your DNA. We sequence it.
FAQ
No. This product is educational and informational only. It is not a diagnostic test, and results should not be used to diagnose, treat, or manage any health condition. Results do not replace clinical testing, medical evaluation, or advice from a qualified healthcare professional.
A Polygenic Risk Score summarizes the combined effect of many genetic variants — often thousands or millions — across your genome that are associated with a particular trait or condition. Rather than looking at a single gene, PRS captures the cumulative influence of common, small-effect variants identified in large genome-wide association studies (GWAS). Your score places you on a risk spectrum relative to the general population.
We currently ship within the United States. International availability is planned for the future — check our website for updates.
Results are typically available 3-4 weeks after your sample is received at our lab. You will receive an email notification when your report is ready to view in your secure account. Please keep in mind that results may take 4-6 weeks if the sample quality is low. Our lab will make two attempts to process each swab before we reach out to you for a new collection.
Wait at least one hour after eating, drinking anything other than water, smoking, chewing tobacco, or using any tobacco or herbal products before swabbing. Immediately before swabbing, rinse your mouth thoroughly with plain water — this is the single most effective step for a high-quality collection, as it significantly reduces non-human DNA (e.g. bacterial content) on the swab. Do not brush your teeth or use mouthwash immediately before swabbing, as this reduces the number of cheek cells collected.
You do. Your genetic data belongs to you. You are empowered to download your data and/or delete your data at any time. We do not claim ownership of your data.
Gencove is a genomics company founded by scientists and engineers with deep expertise in population genetics, bioinformatics, and sequencing technology. Our technology is trusted by research institutions including Stanford and Oxford, as well as pharmaceutical partners like GSK and Boehringer Ingelheim. Our direct to consumer product brings the same sequencing infrastructure — previously available only in research and enterprise settings — directly to consumers.
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Use your genetic baseline to prioritize the actions that matter most.
Start with your baseline