Decode Your DNA.
Discover Your Blueprint.
Upload your raw genetic data and receive professional-grade analysis of health risks, drug responses, carrier status, and traits — all processed privately in your browser.
By the Numbers
Comprehensive Genetic Intelligence
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Genetic Variants Analyzed
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Analysis Categories
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Report Pages
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Private — Data Never Leaves Your Browser
Join 10,000+ users who've decoded their DNA
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Variants Analyzed
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Client-Side Processing
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Genomes Decoded
Comprehensive Analysis
Everything Your Genome Can Tell You
Six powerful modules powered by peer-reviewed research and clinical guidelines — all processed privately in your browser.
Health Risks
Comprehensive analysis of 52+ conditions including cardiovascular disease, diabetes, cancer susceptibility, and neurological disorders backed by GWAS research.
Pharmacogenomics
Know how your body metabolizes medications. Covers CYP2D6, CYP2C19, CYP2C9, VKORC1 and more — based on CPIC clinical guidelines.
Carrier Status
Screen for 10+ recessive conditions including cystic fibrosis, sickle cell disease, Tay-Sachs, and hereditary hemochromatosis.
Traits & Fun Facts
Discover genetic traits like caffeine metabolism, lactose tolerance, muscle composition, taste perception, and 20+ more fun insights.
Ancestry
Explore your ancestral origins using population-informative markers. See your approximate genetic ancestry composition at a glance.
Medication Scanner
Paste your medication list and instantly check for gene-drug interactions. Get color-coded alerts for any pharmacogenomic conflicts.
Simple Process
Three Steps to Your Genetic Blueprint
No account needed. No data stored. Just results.
Get Your Raw Data
Download your raw genetic data file from 23andMe, AncestryDNA, or any service that provides a VCF / text export.
Supports .txt, .csv, and .vcf formats
Upload to GenomeInsight
Drag and drop your file into the browser. Our engine processes everything locally — nothing is ever sent to a server.
Client-side only. Zero network uploads.
Explore Your Report
Instantly view your interactive report covering health risks, drug responses, carrier status, ancestry, and fun genetic traits.
Results in under 10 seconds
See It In Action
Your DNA, Beautifully Decoded
Explore interactive reports that transform raw genetic data into actionable insights.
Health Risks
52 conditions analyzed
Ancestry Map
Global heritage composition
Nutrigenomics
Diet & nutrition insights
Vitamin D
Needs more
Caffeine
Slow metabolizer
Folate (MTHFR)
Supplement recommended
Testimonials
Loved by Users & Clinicians
Real stories from people who decoded their DNA with GenomeInsight.
“Finally understood my MTHFR results after years of confusing reports from other services. GenomeInsight broke everything down into clear, actionable steps. I now take methylfolate instead of regular folic acid — game changer.”
Sarah K.
Health-conscious mom
“The pharmacogenomics report saved me from a bad medication reaction. Turns out I'm a CYP2D6 poor metabolizer — my doctor had no idea until I showed them my GenomeInsight report. Switched meds and feel so much better.”
James R.
Software engineer
“Beautiful interface and incredibly detailed. As a physician, I'm impressed by the scientific rigor. The variant-level data with literature references is exactly what I need for informed conversations with my patients.”
Dr. Lisa M.
Internal Medicine Physician
Pricing
Simple, Transparent Pricing
Pay once, get your complete genetic report forever.
Free
Get started instantly
- Trait analysis (25+ traits)
- Basic ancestry composition
- Raw data browser
- Client-side processing
Essential
Add health insights
- Everything in Free
- Health risk analysis (52 conditions)
- Risk level breakdown
- Category summaries
- Exportable results
Premium
The complete picture
- Everything in Essential
- Pharmacogenomics report (14 genes)
- Medication Scanner
- Carrier status screening
- Clinical-grade PDF export
- Lifetime updates
FAQ
Frequently Asked Questions
Everything you need to know about GenomeInsight.
Absolutely. GenomeInsight processes everything directly in your browser using client-side JavaScript. Your raw genetic data file is never uploaded to any server. No network requests are made with your DNA data. It stays on your device, period.
You can download your raw data from services like 23andMe, AncestryDNA, or MyHeritage. Each provider has a "Download Raw Data" option in their account settings. The file is typically a .txt or .csv file containing your genotyped SNP data.
Our analysis is based on peer-reviewed GWAS (Genome-Wide Association Studies), ClinVar pathogenicity classifications, CPIC pharmacogenomics guidelines, and established population genetics research. However, consumer genotyping covers only a fraction of your genome. Results are informational — not diagnostic.
No. GenomeInsight is strictly an educational and informational tool. It is NOT a medical device, diagnostic test, or clinical service. Genetic risk factors are just one piece of the puzzle — lifestyle, environment, and family history all matter. Always consult a qualified healthcare provider before making medical decisions.
We support raw data exports from 23andMe (.txt), AncestryDNA (.txt), MyHeritage (.csv), and standard VCF files (.vcf). The parser auto-detects the format and extracts SNP data accordingly.
No account is needed. Simply visit the site, upload your file, and get your report instantly. Since everything runs in-browser, there's no sign-up, no login, and no personal information collected.
Pharmacogenomics (PGx) studies how your genes affect your response to medications. For example, variants in CYP2D6 can make you a poor or ultra-rapid metabolizer of certain drugs like codeine or tamoxifen. Our report covers 14 key drug-gene interactions based on CPIC guidelines.
Your genetic data is fixed, but our analysis database grows. As new research is published and we add more variants, re-uploading your file will give you an updated, more comprehensive report. Premium users get lifetime access to all future updates.
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