Stop guessing what your raw DNA file means. Turn it into a usable health report today.
Upload your existing 23andMe, AncestryDNA, MyHeritage, or compatible raw data file. Get personalized reports for drug response, methylation, nutrition, carrier status, and a practical health protocol.
Educational reports only. Not a diagnosis. Discuss medical decisions with qualified clinicians.
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- ✓Generate your full DNA health report after upload
- ✓See drug response, methylation, carrier, and risk context
- ✓Get a protocol-style action plan plus 30-day AI chat access
Pay with Stripe, create your account, upload your raw DNA file, and generate your private reports.
A private report room, not another spreadsheet dump.
Most raw DNA tools make you do the hard part yourself. Your DNA Unlocked organizes findings into sections built for scanning, comparison, and follow-up.
CYP and PharmGKB-informed insights for common drug metabolism pathways.
MTHFR, COMT, vitamin D, caffeine, lactose, and related pathway findings.
ClinVar-based review for pathogenic variants, carrier status, and risk markers.
Diet, supplement, exercise, lab, and monitoring ideas organized into next steps.
Highlights medication response pathways worth reviewing before prescriptions or dosage changes.
Turns genetics into a structured plan for nutrients, habits, labs, and follow-up questions.
Ask your report questions in plain English.
The report gives you the findings. AI chat helps you work through them. Ask what a section means, what to prioritize, what to ask your doctor, or how one pathway connects to another.
Ask for a simpler explanation of any report section.
Ask which findings are most worth reviewing first.
Get a concise list to bring into your next appointment.
Discuss labs, habits, supplements, and follow-up ideas from your protocol.
CYP2C9 (rs1799853) Category: Drug Metabolism Your Genotype: TT Status: Poor Impact: HIGH 4/6 Description: Poor CYP2C9 (2/2) - significant warfarin sensitivity
Your CYP2C9 result (rs1799853 = TT) suggests you are a poor CYP2C9 metabolizer. In plain terms: your body breaks down certain medications more slowly than average, so standard doses can hit harder and last longer.
CYP2C9 is one of the main enzymes that clears warfarin, a blood thinner. With a poor-metabolizer pattern like this, warfarin can build up more easily, which raises the chance of over-anticoagulation and bleeding if dosing is not adjusted. This is a risk tendency, not a diagnosis, but it is clinically important.
If you ever need warfarin: tell your prescriber up front that you have a CYP2C9 poor-metabolizer result. Clinicians can use this, often along with VKORC1 and other factors, to choose a lower starting dose and monitor INR more closely.
AI chat is educational and based on your generated reports. It does not replace medical advice.
A raw DNA file is not valuable until it changes what you understand.
Raw files hide the signal
Your export is built for machines. The report turns markers into named pathways, findings, caveats, and next steps.
Health context beats trivia
The focus is medication response, methylation, nutrition, carrier status, disease-risk context, and protocol planning.
You need a usable next step
The goal is not certainty from one gene. It is a sharper list of what to review, ask, test, track, or rule out.
From raw DNA file to private health report in three steps.
Start secure checkout, create your private account, upload your raw data file, and generate reports you can actually read and use.
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Pay with Stripe. The price you see on this page is the price sent into checkout.
Private account
After payment, create your password and enter your report workspace.
Upload and generate
Upload your raw DNA file and unlock your reports inside the app.
Genetic data is personal. Your report workspace should feel locked down, not casual.
Your uploaded file is used to generate your reports. You can delete uploaded genome files and generated reports from account settings.
Remove uploaded genome files and generated reports from settings.
Use reports to prepare better questions, not to replace medical care.
Checkout unlocks a password-protected report workspace.
Findings are framed with recognized genetics resources and caveats.
The right fit is someone with a raw DNA file and a real question.
This is not a DNA testing kit and it is not a diagnosis. It is a paid interpretation layer for people who want a clearer, more useful read on data they already own.
Which files work?
Raw data exports from major consumer DNA providers such as 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, and LivingDNA.
What happens after payment?
You create your password, upload your raw file in the private app, and generate your unlocked reports.
Is this medical advice?
No. Reports are educational and meant to support informed conversations with qualified clinicians.
What about the AI chat trial?
Full report access includes 30 days of AI chat for discussing your generated reports. Ongoing chat details are handled in the app.
Can I delete my genetic data?
Yes. Account settings include controls to remove uploaded genome files and generated reports.
Is a DNA test included?
No. Your DNA Unlocked interprets an existing raw DNA file. You do not need to buy another kit here.
Unlock the report your raw DNA file should have come with.
Unlock full access for loading price.... Then create your account and upload your file.