Read your DNA. Watch it never leave.
Drop your 23andMe or Ancestry file and get an honest read of it. Every finding graded A to D by strength of evidence, labeled with the ancestry it was proven in, and shown as where you fall against a reference population. Not a diagnosis, and never uploaded.
// the trace below is a
live base-call readout.
your file makes one like it.
0 bytes ever transmitted.
Four numbers we dare you to check.
No dashboard you have to trust, every figure is verifiable from your own browser’s network tab.
What your report actually gives you.
Most reports hand you a pile of traits. We hand you the one thing they hide: how much to trust each number.
A number in an honest unit.
Each score shows where you fall against a reference population, not a disease verdict. We put the real effect in context instead of a scary standalone figure, and treat your genes as one input beside age, family history and lifestyle.
Labeled with where it was proven.
A score built in one ancestry can lose most of its accuracy in another. Every finding is tagged with the ancestry it was validated in, and flagged when it may not apply to you. Never a single global number.
Graded A to D, finding by finding.
A large, replicated result never looks like a single small study on your report. Grades follow the ClinGen and PGS Catalog standards, and every finding cites its source so you can check our work.
Understanding, not a verdict.
Predisposition and plain explanation, never a diagnosis or a drug-response call. We state the limits up front, point you to a clinician for anything health-adjacent, and never attach a supplement upsell.
What a graded result actually looks like.
Three rows from a sample report. The pharmacogenomic rows are CPIC-based and written for your clinician, never as instructions.
| Marker | Finding | Plain reading | Grade |
|---|---|---|---|
| CYP2C19 rs12248560 | Rapid metabolizer | Activates clopidogrel (Plavix) faster than average, worth knowing before that drug is prescribed. | ACPIC 1A |
| VKORC1 rs9923231 | Increased warfarin sensitivity | CPIC associates this variant with increased warfarin sensitivity, informational, for your clinician. | ACPIC 1A |
| CYP1A2 caffeine | Slow metabolizer · 78th pct | Caffeine clears more slowly for you than for most people, a trait signal, not a medical one. | BSeveral studies |
Run a full analysis. Watch nothing leave.
1.18 million SNPs base-called and graded while the network stays silent. Open your own dev-tools alongside it, the request count won’t move.
One price, on the record.
A subscription to your own genome is a billing relationship that never ends, and a standing reason for someone to hold your data hostage.
Verinome is one payment. No account before you upload, nothing recurring, nothing for a future owner to sell.
Your genome, on your terms.
Drop in your file and see it graded, free to try, on your device, in under a second.