How it works

Six simple steps.

No lab coats. No jargon. Just a careful, warm reading of the genes that come up most often in wellness conversations.

  1. 01

    Download your raw file

    From 23andMe or AncestryDNA. It's a small text file you already own.

  2. 02

    Upload securely

    Encrypted the moment it leaves your device. You can delete it right after we read it.

  3. 03

    We check the file

    We confirm the company, genome build, and quality before we read a single gene.

  4. 04

    We look up curated genes

    About 30 well-studied SNPs — MTHFR, COMT, DAO, the CYPs, VDR, APOE, TCF7L2, and more.

  5. 05

    You read your chapters

    Written in plain, everyday language with what this may suggest AND what it does not tell us.

  6. 06

    You get questions to ask

    Each result comes with 2–3 clear questions worth raising at your next visit.

What you actually walk away with

Target your genes

A supplement list built from your file, not from a magazine article.

Shorten the shopping list

Multi-ingredient products first, so three bottles do the work of nine.

Know your medications

Liver enzymes like CYP2C19 and CYP2D6 change how fast some drugs clear.

Own the conversation

Walk into your appointment with specifics instead of a vague complaint.

Files we can read

Any standard microarray raw data file, zipped or plain text.

23andMeAncestryDNAMyHeritagetellMeGenLifeDNAFitnessGenesMyHappyGenesGenomeitall

Want the background first?

Start with why genetic profiling is worth doing, then read the MTHFR and COMT explainers.