YourDNAholdsanswers.Wedecodethem.
Get an AI-powered health report from your DNA. 576 variants, 88 medications, 60 risk scores — not the 2% others test.
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ClinVar
PharmGKBgnomADStanfordNatureHarvardMITOpenAIArc InstituteUC BerkeleyCambridgeNIHBroad InstituteUCSFEMBL-EBISangerHuggingFaceClinVarPharmGKBgnomADDiscover what's hiding in your DNA
11 dimensions of your health — from cancer screening to drug response — decoded from a single sample.
Not just data. Answers.
Here's what you'll find in your report.
One score. Your whole genome.
596 genetic markers analyzed, 60 polygenic risk scores calculated, distilled into a single number that tells you where you stand. Green means go. Orange means watch. Red means act.
Clear actions. Not guesswork.
Other tests give you raw data and say "talk to your doctor." We tell you exactly what to discuss — ranked by urgency.
Poor metabolizer — codeine & tramadol won't work for you
Elevated Alzheimer's risk — lifestyle changes can reduce it by 40%
Reduced folate metabolism — consider methylfolate supplement
Will your medications work?
88 medications checked against your DNA. For each one: will it work, does it need a dose adjustment, or should you avoid it entirely. Print it and bring it to your next appointment.
Get your drug response reportA roadmap for every decade.
Your DNA doesn't change, but what matters at 30 is different from what matters at 50. We map out what to watch — and when — so nothing catches you off guard.
- Inform doctor re: CYP2D6
- Start methylfolate
- Cardiovascular screening
- Cholesterol monitoring
- Cognitive health check
- Annual skin screening
We found 3 things others missed.
Our AI scanned 50,000+ positions in your genome that no traditional test covers. It found 3 variants worth your attention — variants that would have been labeled "unknown" everywhere else.
Three steps to decode your genome
From upload to insight in as little as 24 hours
Upload or Order
Upload your existing raw DNA file or order a premium saliva collection kit delivered to your door.
AI Analysis
Our Evo2-powered engine analyzes 98% of your genome — not just the 2% traditional tests cover.
Your Report
A comprehensive, actionable report with health risks, drug response, and ancestry insights.
An AI that reads DNA.
That didn't exist before.
Until now, computers could only look at the 2% of your DNA that science already understood. Our AI scans all of it — including mutations that standard DNA chips physically cannot detect.
We scan every letter of your DNA
Your DNA is a sequence of 3 billion letters. Traditional tests only read 2% of them — the parts science already understands.
Our AI was trained on the DNA of every living species on Earth. It learned what "normal" DNA looks like — so it can spot when something in yours is different.
Traditional tests
Read ~20,000 known spots. Ignore the rest.
Our AI analysis
Reads everything. Flags anything unusual.
Powered by Evo2, the largest DNA language model — trained on 3.2 trillion genetic letters from bacteria, plants, animals, and humans.
It spots the "typos"
When a letter in your DNA is different from what the AI expects, it raises a flag — like finding a spelling mistake in a legal document.
Like a typo in a sentence that changes the meaning entirely.
Then we investigate what it means
A "typo" in your DNA doesn't always mean something bad. So we check it against the world's largest medical databases to understand if it matters — and why.
Is this change known?
We check against 2 million classified changes from hospitals worldwide.
ClinVar — NIH database
What does research say?
We look at 313,000 studies linking DNA changes to health conditions.
GWAS Catalog
How rare is it?
We compare yours against 6.8 million people. Rare changes deserve more attention.
gnomAD population data
Has nature ever touched it?
If this spot hasn't changed across species in 100 million years, it's probably important.
Cross-species conservation
You get a clear answer
Other tests say "unknown significance" on most of your results.
We combine the AI's detection with medical databases to give you a plain-language explanation — what was found, what it might mean, and what to discuss with your doctor.
That's why we catch things others miss — including changes never seen before.
Real people. Real insights.
Real people, real insights from their genomic analysis
“After years of trying different antidepressants, I finally understood why none of them worked. Turns out I'm a poor metabolizer for most SSRIs. Brought the report to my psychiatrist and we found the right one in weeks instead of months.”
Rachel K.
Portland, OR
“I was nervous about uploading my DNA anywhere after the 23andMe bankruptcy. The fact that the file never leaves my browser made me actually go through with it. And the report was way more useful than what 23andMe ever gave me.”
Daniel S.
London, UK
“I'd been dealing with brain fog for years. The report showed I have a slow COMT variant — my doctor had never tested for it. Changed my supplement routine and I genuinely feel sharper.”
Megan T.
Austin, TX
“I tried uploading my raw data to ChatGPT first. It told me I had three diseases I definitely don't have. This report actually cites real medical databases for every finding. Night and day difference.”
James L.
Toronto, CA
“My mom had breast cancer, so I was terrified of my BRCA results. What I appreciated is that the report didn't just scare me — it told me exactly which screenings to request and what to ask my doctor. That's what I needed.”
Sofia N.
Barcelona, ES
“I'm a naturopath and I've used Promethease, SelfDecode, and PureGenomics with patients. This is the first report I don't need to translate into English for them. They actually understand it.”
Dr. Laura H.
Denver, CO
“My Promethease report just vanished one day — they deleted everyone's files and wanted me to pay again. Switched to this and honestly the report is 10x more useful. Promethease just gave me a wall of data I couldn't read.”
Alex W.
Chicago, IL
“I've been dealing with chronic fatigue and my doctor couldn't figure it out. Report showed MTHFR C677T homozygous — my body wasn't converting folate properly. Started methylfolate and within two weeks I felt like a different person.”
Hannah B.
Melbourne, AU
“My wife and I used this before planning our second child. Found out we're both carriers for a recessive condition we had no idea about. Our genetic counselor said the report was thorough enough to work from directly.”
Kevin D.
Amsterdam, NL
“I'm a biohacker and I've spent years optimizing supplements based on guesswork. This report finally gave me the actual data — slow COMT, fast MAO-A, poor methylation. Now my stack is based on my genes, not Reddit threads.”
Chris M.
San Diego, CA
“I was paying $120/year for SelfDecode and half the results said 'insufficient data.' This was a one-time payment and covered everything including pharmacogenomics. No subscription, no upsells. Exactly what I wanted.”
Priya S.
New York, NY
“Codeine literally does nothing for me — I always thought I was being dramatic. Report confirmed I'm an ultra-rapid CYP2D6 metabolizer. Printed the drug table and my doctor immediately switched my pain management plan.”
Tom R.
Dublin, IE
“After years of trying different antidepressants, I finally understood why none of them worked. Turns out I'm a poor metabolizer for most SSRIs. Brought the report to my psychiatrist and we found the right one in weeks instead of months.”
Rachel K.
Portland, OR
“I was nervous about uploading my DNA anywhere after the 23andMe bankruptcy. The fact that the file never leaves my browser made me actually go through with it. And the report was way more useful than what 23andMe ever gave me.”
Daniel S.
London, UK
“I'd been dealing with brain fog for years. The report showed I have a slow COMT variant — my doctor had never tested for it. Changed my supplement routine and I genuinely feel sharper.”
Megan T.
Austin, TX
“I tried uploading my raw data to ChatGPT first. It told me I had three diseases I definitely don't have. This report actually cites real medical databases for every finding. Night and day difference.”
James L.
Toronto, CA
“My mom had breast cancer, so I was terrified of my BRCA results. What I appreciated is that the report didn't just scare me — it told me exactly which screenings to request and what to ask my doctor. That's what I needed.”
Sofia N.
Barcelona, ES
“I'm a naturopath and I've used Promethease, SelfDecode, and PureGenomics with patients. This is the first report I don't need to translate into English for them. They actually understand it.”
Dr. Laura H.
Denver, CO
“My Promethease report just vanished one day — they deleted everyone's files and wanted me to pay again. Switched to this and honestly the report is 10x more useful. Promethease just gave me a wall of data I couldn't read.”
Alex W.
Chicago, IL
“I've been dealing with chronic fatigue and my doctor couldn't figure it out. Report showed MTHFR C677T homozygous — my body wasn't converting folate properly. Started methylfolate and within two weeks I felt like a different person.”
Hannah B.
Melbourne, AU
“My wife and I used this before planning our second child. Found out we're both carriers for a recessive condition we had no idea about. Our genetic counselor said the report was thorough enough to work from directly.”
Kevin D.
Amsterdam, NL
“I'm a biohacker and I've spent years optimizing supplements based on guesswork. This report finally gave me the actual data — slow COMT, fast MAO-A, poor methylation. Now my stack is based on my genes, not Reddit threads.”
Chris M.
San Diego, CA
“I was paying $120/year for SelfDecode and half the results said 'insufficient data.' This was a one-time payment and covered everything including pharmacogenomics. No subscription, no upsells. Exactly what I wanted.”
Priya S.
New York, NY
“Codeine literally does nothing for me — I always thought I was being dramatic. Report confirmed I'm an ultra-rapid CYP2D6 metabolizer. Printed the drug table and my doctor immediately switched my pain management plan.”
Tom R.
Dublin, IE
“After years of trying different antidepressants, I finally understood why none of them worked. Turns out I'm a poor metabolizer for most SSRIs. Brought the report to my psychiatrist and we found the right one in weeks instead of months.”
Rachel K.
Portland, OR
“I was nervous about uploading my DNA anywhere after the 23andMe bankruptcy. The fact that the file never leaves my browser made me actually go through with it. And the report was way more useful than what 23andMe ever gave me.”
Daniel S.
London, UK
“I'd been dealing with brain fog for years. The report showed I have a slow COMT variant — my doctor had never tested for it. Changed my supplement routine and I genuinely feel sharper.”
Megan T.
Austin, TX
“I tried uploading my raw data to ChatGPT first. It told me I had three diseases I definitely don't have. This report actually cites real medical databases for every finding. Night and day difference.”
James L.
Toronto, CA
“My mom had breast cancer, so I was terrified of my BRCA results. What I appreciated is that the report didn't just scare me — it told me exactly which screenings to request and what to ask my doctor. That's what I needed.”
Sofia N.
Barcelona, ES
“I'm a naturopath and I've used Promethease, SelfDecode, and PureGenomics with patients. This is the first report I don't need to translate into English for them. They actually understand it.”
Dr. Laura H.
Denver, CO
“My Promethease report just vanished one day — they deleted everyone's files and wanted me to pay again. Switched to this and honestly the report is 10x more useful. Promethease just gave me a wall of data I couldn't read.”
Alex W.
Chicago, IL
“I've been dealing with chronic fatigue and my doctor couldn't figure it out. Report showed MTHFR C677T homozygous — my body wasn't converting folate properly. Started methylfolate and within two weeks I felt like a different person.”
Hannah B.
Melbourne, AU
“My wife and I used this before planning our second child. Found out we're both carriers for a recessive condition we had no idea about. Our genetic counselor said the report was thorough enough to work from directly.”
Kevin D.
Amsterdam, NL
“I'm a biohacker and I've spent years optimizing supplements based on guesswork. This report finally gave me the actual data — slow COMT, fast MAO-A, poor methylation. Now my stack is based on my genes, not Reddit threads.”
Chris M.
San Diego, CA
“I was paying $120/year for SelfDecode and half the results said 'insufficient data.' This was a one-time payment and covered everything including pharmacogenomics. No subscription, no upsells. Exactly what I wanted.”
Priya S.
New York, NY
“Codeine literally does nothing for me — I always thought I was being dramatic. Report confirmed I'm an ultra-rapid CYP2D6 metabolizer. Printed the drug table and my doctor immediately switched my pain management plan.”
Tom R.
Dublin, IE
Drag to explore→
Start with what you have
From quick insights to complete genome analysis
Upload Report
Already have your DNA file?
Upload your existing 23andMe, AncestryDNA, or VCF file and get an AI-powered health report in 2 minutes. No kit needed.
- 23andMe, AncestryDNA, MyHeritage, VCF
- 576 variants across 15 categories
- 88 medication interactions
- 60 polygenic risk scores
- Personalized nutrition insights
- Doctor-ready PDF with references
- Instant results
DNA Kit + Report
Don't have a DNA file? We handle everything.
We ship a saliva collection kit to your door. Full genome sequencing included — the most complete DNA health report available.
- Saliva kit shipped to your door
- Prepaid return envelope
- Full genome sequencing (30× coverage)
- 576+ variants analyzed by AI
- 88 medication interactions
- 60 polygenic risk scores
- Personalized nutrition insights
- Doctor-ready PDF with references
- Results in ~2-3 weeks
What's included in every plan
Premium DNA collection
Designed for simplicity. Medical-grade quality.
Open
Unbox your premium kit
Collect
2-minute saliva sample
Ship
Drop in any mailbox
Questions? Answered.
Still have questions?
Our team is here to help. Reach out and we'll get back to you within 24 hours.
Your DNA never leaves your control
We don't store, sell, or share your genetic data. Ever. Analysis happens in an encrypted pipeline and data is deleted after your report is generated.
End-to-End Encryption
Your genomic data is encrypted using AES-256 from the moment you upload it. Even we can't read your raw data.
GDPR & HIPAA Compliant
We follow the strictest data protection standards. Your genetic information is classified as sensitive personal data and treated accordingly.
Automatic Deletion
After your report is generated, raw genomic data is permanently deleted from our servers. You keep the insights, we keep nothing.
Trusted by researchers at
StanfordHarvardMITBroad InstituteArc InstituteYour genome is waiting.
Join thousands who've discovered what their genome reveals about their health, ancestry, and future.
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