Privacy-First DNA Analysis
Your DNA.
Your Device.
Your Insights.
Upload your raw DNA file and get comprehensive health, trait, and ancestry analysis — all processed locally in your browser. Your genetic data never leaves your device.
One-time payment. No subscription. No data stored.
How It Works
Three simple steps from purchase to personalized genetic insights.
Pay Once
Secure one-time payment of $49 via Stripe. No subscriptions, no hidden fees. You get lifetime access to your analysis.
Upload Your File
Drop your raw DNA file from 23andMe, AncestryDNA, or other services. The file is processed entirely in your browser — nothing is uploaded to any server.
100% Browser-BasedGet Your Results
Receive comprehensive health risks, pharmacogenomics, traits, carrier status, ancestry breakdown, and a downloadable PDF report — instantly.
Privacy by Architecture
Your genetic data never touches our servers. This is not a policy promise — it is a technical guarantee.
Input
Raw DNA File
23andMe, AncestryDNA, etc.
Processing Engine
WebAssembly Analysis
ClinVar, PharmGKB, trait databases — all bundled in WASM
Output
Health, Traits, Ancestry & PDF
Displayed in your browser, downloadable as PDF
All data stays here. Nothing leaves.
Only Function
Payment Processing
Stripe handles all payment securely
Not Stored
No DNA data
No analysis results
No personal health info
Zero access to your genetic data.
What You Get
Comprehensive genetic analysis covering health, pharmacogenomics, traits, ancestry and more — all from a single DNA file.
Health Risk Analysis
Screen for genetic variants linked to conditions like heart disease, diabetes, Alzheimer's and more. Powered by the ClinVar clinical database.
Pharmacogenomics
Discover how your DNA affects drug response. Learn which medications may work better — or worse — based on your genetic makeup.
Trait Analysis
Explore physical and behavioral traits influenced by your genetics — from caffeine metabolism to muscle composition to sleep patterns.
Carrier Status
Find out if you carry recessive variants for conditions like cystic fibrosis, sickle cell disease, or Tay-Sachs that could affect future children.
Ancestry Estimation
Get a breakdown of your ancestral population composition based on thousands of ancestry-informative markers across your genome.
Interactive Karyogram
Visualize your results on a chromosome-by-chromosome genome map. Click any chromosome to explore the variants found there.
PDF Report Download
Generate a comprehensive, print-ready PDF report of all your findings. Share with your doctor or keep for personal records.
Sample Results Preview
Here is what your analysis report looks like. Real findings, clearly presented with clinical context.
Health Risk Analysis
ClinVar-powered variant screening
Hereditary Breast & Ovarian Cancer
Pathogenic variant detected. Discuss with a genetic counselor.
Codeine Poor Metabolizer
Reduced enzyme activity. Codeine may be less effective.
Lactose Tolerance
Lactase persistence variant detected. Likely lactose tolerant.
Alzheimer Disease Risk
APOE e4 carrier. Associated with increased late-onset AD risk.
This is a preview with sample data. Your actual report will contain findings based on your unique DNA.
Simple Pricing
One payment. Full analysis. No subscriptions.
One-Time Payment
No recurring charges. Ever.
- ✓Health risk screening (ClinVar database)
- ✓Pharmacogenomics drug response analysis
- ✓Trait analysis (physical & behavioral)
- ✓Carrier status for recessive conditions
- ✓Ancestry population estimation
- ✓Interactive chromosome karyogram
- ✓Downloadable PDF report
- ✓100% browser-based processing
- ✓No data stored on any server
- ✓Lifetime access to your results
Secure payment via Stripe. Instant access after purchase.
Frequently Asked Questions
Yes. Your DNA file is processed entirely within your web browser using WebAssembly. The file is never uploaded to any server. We have zero access to your genetic data — this is enforced by the architecture, not just a policy. Only your payment information is handled server-side via Stripe.
We support raw data files from 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, and most other direct-to-consumer genetic testing services. The file is typically a .txt or .csv file that you can download from your testing provider's website.
Analysis typically completes in 30 to 90 seconds, depending on your device and file size. The WebAssembly engine is optimized for performance and runs natively in your browser at near-native speed.
No. ReadMyDNA provides genetic information for educational and informational purposes only. Results should not be used to diagnose, treat, or prevent any medical condition. Always consult a qualified healthcare professional or genetic counselor before making health decisions based on genetic data.
If you encounter any issues with the analysis or have questions about your results, you can reach our support team via the contact link in the footer. We typically respond within 24 hours.