Your genome, read with editorial care.

Genomics, taken whole, is still a young science, and we don't pretend otherwise. Varia reports only the fraction of your genome where peer-reviewed evidence is strong enough to stand on, drawn from the Tier 1 and Tier 2 journals our Varia Evidence Grading Schema (VEGS) is built on. The result is fewer findings, where each one can actually matter to your health, and each carries the leading evidence behind it.

Every finding traced to peer-reviewed evidence

NEJM · JAMA · Nature · Cell · ClinVar · CPIC

Your DNA file is read in your browser and never leaves your device. Varia keeps no scan results, so each visit you reload your file and rescan in seconds. How your data is handled

Private by design, not by promise

Your DNA is read in your browser, never uploaded. We can't sell, leak, or lose a genome we never receive, and we keep only your name, email, and unlock status.

Privacy policy

If we cannot cite it, you will not see it

Every finding traces to a top-tier journal: NEJM, JAMA, Nature, Cell. No SNPedia, no forum lore, no anecdotes.

How we grade evidence

Made for your doctor, not your supplement cabinet

Findings and citations to bring to your next appointment. Information to inform care with your physician, never a prescription to self-treat.

Read the medical disclaimer

How it works

1. Load your file. It is read in your browser, never uploaded.
2. See a free preview. Confirm the scan worked, no findings revealed.
3. Unlock the full read. $12 founding rate for the first 100 unlocks, $29 after.

Free scan and preview. Your scan confirms your file processed and shows how many variants we found across your domains. $29 unlocks your interactive dashboard and Varia Genomic Brief.

The first 100 unlocks are $12 (founding rate); then $29 one-time. Free scan and preview always. See pricing.

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