Have your 23andMe or AncestryDNA raw file?

Before you buy that supplement,ask your actual DNA.

Paste your raw DNA file and get a decision for your variants — not population averages. Which form fits you, what to be careful with, and an overmethylation safety flag. Your first question is free.

🔒 Works with 23andMe, Ancestry & 100+ more🇪🇺 Delete your data anytimeFirst question free — no card
Ask My DNA
AI Ready
Ask your DNA anything...

A report explains your genes. ChatGPT guesses from averages. Neither decides for you.

We read your real genotypes from your file and answer the question you have right now

Reports & generic AI
Ask My DNA
Static 30-trait report to interpret yourself
A decision for the exact question you have now
ChatGPT can't load your 20 MB DNA file
We pull your real genotypes straight from it
One gene, one row at a time
Your COMT + MTHFR read together
Generic "ask your doctor"
A safe starting point + overmethylation flag

Try it before you pay a cent

1st question

Free — no card

Then 5 for $5

One-time pack, no subscription

Ask again anytime

Every time you buy your next supplement

Why the answer is about you — not the average person

Every answer is built from your own file in three steps.

📤
Step 1

You ask

Type a real question — "Is methylfolate right for my MTHFR, or will it overmethylate me?" We pick the exact markers it depends on (rs1801133, rs4680, MTRR…).

💬
Step 2

We read your file

We extract your actual genotypes from your uploaded raw data — the real variants out of 600,000+ SNPs, not a fixed panel.

💡
Step 3

You get a decision

An answer for your specific variants — which form and starting point, with a safe / caution / avoid overmethylation flag. Plain ChatGPT can't load your file; static reports can't do this.

⚠️ Overmethylation safety

Crashed on methylfolate before? That's exactly why the flag exists.

If your COMT is slow, methyl donors can tip you into overmethylation — anxiety, insomnia, irritability. We read that against your own file and flag safe / caution / avoid before you dose, so your next bottle doesn't set you back.

Educational, not medical advice. We don't prescribe doses — we help you ask sharper questions of your own genetics and your doctor.

One question, answered from your file — across your genes

The same personal read, whatever supplement decision you're facing today

🧬

Methylation

"Is methylfolate right for my MTHFR + COMT — or will it overmethylate me?"

Caffeine

"Am I a slow CYP1A2 metabolizer — how much coffee, and how late?"

🧠

Mood & dopamine

"Slow COMT and MAOA — which supplements help, which push me over?"

🛡️

Detox

"GSTM1 null — should I take NAC, glutathione, or sulforaphane?"

☀️

Vitamin D

"VDR variant — why does D never work for me, what dose and form?"

🌡️

Histamine

"DAO or HNMT — why do I react, and what actually helps?"

Built for people who already know their genes

If you have a raw DNA file and a supplement decision, this is for you

The methylator

"I need to know if methyl-B's fit my COMT before I dose them"

🌀

The over-sensitive

"I've crashed on methylfolate — I need an overmethylation check first"

🔬

The optimizer

"I want to stop guessing which supplements actually fit my genotype"

🧫

The self-experimenter

"I read r/MTHFR and I want answers from my own file, not averages"

What people found in their own file

I spent 2 years wondering why vitamin D never worked for me. It flagged a VDR variant that needs D3 with K2 and magnesium. My levels finally normalized.

S

Sarah M.

Biohacker, California

I kept crashing on methylfolate — anxiety, no sleep. It read my slow COMT and pointed me to a lower dose and a non-methyl form. The anxiety stopped.

M

Marcus T.

Self-experimenter, Austin

Asked why coffee gives me anxiety when my husband drinks 4 cups fine. I'm a slow CYP1A2 metabolizer — switched to one cup before noon and my sleep came back.

E

Elena K.

Software engineer, New York

Questions answered across MTHFR, COMT, CYP1A2, VDR and more

by biohackers reading their own raw DNA files

Backed by research, private by design

GDPRCompliant
PubMedNCBI / NIH
ClinVarNIH Database
EncryptedAES-256

Peer-reviewed genetics databases, encrypted, never sold — delete anytime

Your next supplement decision is already in your DNA file.

Upload your raw data from any testing service and ask your first question free — a personal answer in under 60 seconds. Private and encrypted.

🔒 Works with 23andMe, Ancestry & 100+ moreDelete your data anytimeFirst question free — no card

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