Already took a DNA test? Here's the part they left out.
Upload the raw file you already have. In minutes, we cross-reference your genetic variants — the individual DNA markers called SNPs — against ClinVar, PharmGKB, the GWAS Catalog and other public databases, and turn it all into one clear, illustrated report of what your DNA actually means.
Create a secure account
Sign up with email + password and verify it via a one-time code. We strongly encourage enabling two-factor authentication. You must confirm you're 18 or older.
Subscribe — your first report is free
Report Update Monitoring is $9.99/mo, billed $29.99 every quarter via Stripe from your start date. Subscribing unlocks your first DNA upload and your full Genetic Profile — all report types included — free, plus monthly update checks as new science emerges. A US-resident confirmation is required.
Upload your raw DNA file
After subscribing, export a raw-data file from 23andMe, AncestryDNA, MyHeritage, or FamilyTreeDNA. We accept .txt, .csv, and .zip up to 50MB and auto-detect the vendor and genome build (GRCh37 / GRCh38); VCF/BAM are politely rejected. Optionally tick “Keep my raw file for future re-analysis” (off by default — if left off, your raw file is deleted 30 days after your report is generated). Then complete the mandatory informed-consent checklist to begin.
We analyze your DNA
A checkpointed, rate-limited pipeline cross-references every annotated variant against ClinVar, the GWAS Catalog, PharmGKB, dbSNP, Ensembl, gnomAD, GenCC, HPO, MedlinePlus, ClinGen, and Google Scholar. It typically takes a few minutes — you can stay on the page or safely leave; we email you the moment your report is ready, and it also appears in My Reports.
Explore & export your report
Fun facts first, then health, pharmacogenomics, carrier status, traits, nutrigenomics, fitness, sleep, longevity, and ancestry — each section appears only where your data has findings, with sensitive findings behind an opt-in reveal. Download a PDF or HTML copy, search and filter by category, or share a fun fact.
Stay current with monitoring
Include any report you want in monitoring (off by default). Each month we check whether new research changes any of your included SNPs; meaningful changes surface in your Dashboard's Since Your Last Visit and are summarized in your monthly monitoring digest. Cancel anytime — your reports stay viewable forever, and resubscribing resumes updates from the next monthly check.
Ready to decode your DNA?
$9.99/mo · billed $29.99 quarterly · your first report free.