How it works
From raw DNA file to personalised insights — in minutes.
A transparent, evidence-linked pipeline. Every insight shows the variant, the source, and when it was last reviewed.
- Step 1
Upload your raw DNA
Drag and drop the raw data file from 23andMe, AncestryDNA, MyHeritage, or FamilyTreeDNA. Format is detected automatically.
- Step 2
AI analyses your variants
Our pipeline parses ~600,000 SNPs and cross-references curated, peer-reviewed sources including ClinVar, gnomAD, and PharmGKB.
- Step 3
Receive personalised reports
Health risk, pharmacogenomics, ancestry, and rare disease screening — each insight cites its evidence and reviewer.
Not medical advice. AI-generated insights are educational only. Always verify with a qualified healthcare professional.