people carry a genetic finding worth acting on, and nearly four in ten of them do not know.
cohort studyHealth layer built
on your DNA
Upload your DNA file and get personalised, science-backed
guidance that keeps improving.
23andMeAncestryDNAMyHeritageTellMeGenWGS/VCF
Thyroid, stress & reproductive balance
Find the signal inside your DNA
It shapes how your body processes nutrients, responds to exercise and recovers.
We translate that into evidence you can act on.
carry a variant that changes how they respond to a commonly prescribed medicine.
cpic / pharmgkbcarry a common MTHFR variant that can influence how they process folate.
cdc / nihis all you sequence. Your DNA never changes; what science can read in it keeps improving.
clinvarof variants make each genome unique. Most have little known impact; a few genuinely matter.
nhgriFrom raw DNA to clear actions
Upload
Upload the raw-data file from your existing DNA provider.
Verify
We match supported variants against our evidence layer, on your device.
Understand
Receive a personalised preview, then unlock your full layer.
Act
Improve your health with the action plan and the agentic report.
Your DNA never leaves your device. Only anonymous derivatives reach the model.
About 0.5% of the fileAction plan
The thirteen areas we cover, and what to do about each of them.

You may benefit from more vitamin D. Your baseline levels are genetically lower.
Agentic report
Importable into any AI, and built to beat what a chatbot can tell you about your DNA.
more variants covered
more findings
Outperforming top LLMs
Built for trust
Your DNA is sensitive, and genetic findings are rarely absolute. We protect the underlying data and stay clear about what the evidence can and cannot tell you.
Private by design
Your DNA is processed locally, never sold, and stays under your control.
Verified before explained
AI explains verified findings. It does not guess what your raw DNA contains.
Evidence without overclaiming
Every finding carries its evidence strength, its sources and its limitations.
DNA Layer is for informational and educational use only. It does not diagnose, treat, or prevent any disease. Important findings may require confirmation in a clinical laboratory and review by a qualified healthcare professional.
Your DNA is already written. Start reading it.
No new test required/Free personalised preview
Before you upload anything
No. DNA Layer is built for the raw data file from a test you have already taken. If you have never tested, any of the supported consumer providers will do.
Raw text exports from 23andMe, AncestryDNA, MyHeritage and TellMeGen, plus whole-genome and whole-exome VCF files. Coverage differs between providers, and we tell you which findings your file could and could not support.
A free personalised preview straight after upload. Then, if you unlock it, your full layer: thirteen areas of your health, each finding sorted into strengths, things to try and things worth attention, an action plan, and the agentic report file.
Variant matching runs in deterministic software against a curated evidence layer, so the same file always produces the same findings. Language models only explain findings that have already been verified, never the raw file.
No. Most findings shift a probability rather than settle an outcome, and lifestyle, environment and chance all still apply. That is why evidence strength and limits sit next to every claim.
Your file is read locally in your browser. We keep the minimum needed to show your layer, we never sell genetic data, and you can delete everything from your vault whenever you want.