“I want to understand my 23andMe or AncestryDNA results.”
This is for you if: You already have a raw DNA file and no idea what any of it means.
- 1Upload your genome.
Drag in the .txt or .zip file from 23andMe or AncestryDNA. Nothing leaves your device without your say-so. In about a minute you’ll see two lists: your Strengths and your Things To Be Aware Of, each in one plain sentence.
Why this matters — Because a wall of rs-numbers is useless. Two short lists you can actually read are not.
- 2Read each finding for what it is.
Every finding is framed as a tendency, not a verdict. You’ll see how common it is, an evidence tier for the science behind it, and the papers we’re relying on. Nothing hidden.
Why this matters — So you leave with understanding — not fear and not false certainty.
- 3Turn findings into questions worth asking.
Your Health Blueprint groups findings into pillars (energy, sleep, methylation, etc.) and suggests experiments and questions you can bring to a practitioner — not prescriptions.
Why this matters — Because the next honest step is a better conversation with a real clinician.