Upload your raw DNA file. Add your labs if you have them. Get a personalized protocol our team stands behind.
Most platforms read DNA alone or labs alone. Gene Atlas weaves your DNA, your blood markers, and your goals into one coherent picture.
Most DNA services hand you 200 disconnected gene cards. Gene Atlas reads how your traits interact, where they cluster, and what that means for the goals you actually care about. Each trait is scored across many variants, not one gene.
Export your raw data file from 23andMe, Ancestry, MyHeritage, or LivingDNA.
Drag and drop your file. We process it privately, in minutes.
Read your genetic profile, see your priorities, follow your daily plan. Add labs anytime to sharpen the picture.
Genetic data is the most sensitive file you'll ever upload. Our defaults assume that — and stay that way whether or not you ever read this page.
Your raw DNA file is encrypted in transit and at rest and stored de-identified. Delete your file and your whole account in two clicks, anytime — and anything you don't delete is removed automatically after 180 days of account inactivity.
Not to insurers, not to pharma, not to anyone. No third-party trackers or ad pixels run on your report — what you see is between you and our team.
"Gene Atlas finally explained my workout plateau. The action plan made my programming click, and my daily protocol kept me consistent. I'm recovering faster and PRs are back. Seriously impressed."
"Upload took 2 minutes. The report is clean, easy to read, and the action plan is practical. The habit recommendations made late-night snacking way easier to control."
"I was wasting money on random supplements. The protocol showed what I actually need and what to skip. I saved a ton, and my energy is way steadier (no 3pm crash)."
"The report nailed my focus pattern so well it was spooky. The action plan helped me stop bouncing between tabs and finish tasks. My workdays feel calmer."
"I like that it's not just scary risk labels. The plan feels optimistic and doable. I'm making small changes without overthinking, and it actually sticks when life gets busy."
Gene Atlas reads your DNA file and evaluates many genetic variants per trait simultaneously, rather than relying on any single "predisposition gene." Each variant is matched to its measured association with a given trait, and these weighted contributions are aggregated into a single predisposition score — the same methodology used to construct polygenic risk scores (PRS) in human genetics research. The score reflects your relative predisposition compared to the general population, not an absolute probability of any outcome.
Data sources. All associations are drawn from open, peer-reviewed science — not a closed proprietary dataset. GWAS Catalog (EMBL-EBI / NHGRI), the largest public repository of genome-wide association studies, is the source of risk alleles, effect sizes, and reported traits. The Open Targets Platform (EMBL-EBI, Wellcome Sanger Institute, and partners) contributes variant-to-gene mapping via Locus-to-Gene (L2G) scoring. PubMed, the peer-reviewed biomedical literature, is used to independently cross-check associations.
Evidence and confidence. Each association is weighted by the strength of its underlying evidence: discovery cohort size (N), statistical significance (p < 5×10⁻⁸), independent replication across studies, and consistency of effect direction. Associations with small samples, single-study support, or conflicting directions are down-weighted, so every score carries a transparency rating reflecting how robust its supporting evidence is.
Gene Atlas provides educational, wellness-focused genetic insights. It is not a medical diagnosis or a substitute for advice from a licensed healthcare provider.
Your DNA is your lifelong baseline. Your blood markers, symptoms, and goals show what's happening right now. Gene Atlas connects all of it into one picture and one prioritized plan — and keeps it current as you add new lab results and track what works.
Read about our research approach →