One genome,
three ways to understand it.
A single grounded knowledge base behind every reply. Choose the experience that speaks your language — the science underneath never changes.
Plain-English answers about your health. No jargon, nothing scary — just clarity.
Clinical-grade interpretation. ClinVar and ACMG verbatim, structured for the visit.
Full-fidelity variant data. Query, filter, export — every row, every annotation.
One finding, told three ways
The same SERPINA1 result from the same report. Switch the audience — watch the wording change while the gene, verdict and numbers stay identical.
You have a change in SERPINA1 — a gene that helps protect your lungs. It's linked to a condition that can affect the lungs and liver, so it's worth a chat with your doctor. It doesn't mean you're unwell today.
How the one base works
WGS, WES, clinical CSV, InterVar TXT, or a microbiome panel. Parsed on our servers, never shared.
Every answer is anchored to your actual rows — ClinVar, ACMG evidence, zygosity, scores. No invented variants.
The same verified facts, rendered for your role. Wording changes; genes, verdicts and numbers never do.
A deterministic validator strips any variant or classification that can't be matched to your report.
ClinVar and InterVar verdicts are quoted verbatim — never softened, never upgraded.
Your data is never used to train a model, and is deleted on request. HIPAA-conscious from day one.
Find your way in
Pick the experience that fits — you can always switch. One report, one truth, three voices.