Your DNA. Decoded.

Upload your DNA raw data from any testing service — 23andMe, AncestryDNA, MyHeritage, FTDNA, or VCF — and get actionable health insights in minutes.

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What You Get

Comprehensive genetic analysis powered by clinical databases

Drug Metabolism

12 pharmacogenomic markers that affect how you process medications — caffeine, statins, blood thinners, opioids, and more.

Carrier Screening

Scan against 341,000+ clinical variants from ClinVar. Know your carrier status for recessive conditions.

Lifestyle Genetics

79 SNPs across 16 categories including fitness, nutrition, sleep, cardiovascular, and longevity.

Drug Interactions

PharmGKB-powered analysis of how your genes interact with common medications.

Results in Minutes

Automated analysis pipeline delivers your report within minutes, not weeks.

Privacy First

Raw data deleted immediately after processing. We never store, share, or sell your genetic information.

Choose Your Report

From quick drug metabolism cards to comprehensive genome analysis

Drug Metabolism Card

Discover how your genes affect drug metabolism. Get a personalized card showing how you process caffeine, statins, blood thinners, opioids, antidepressants, and more. Based on …

$14.99 View Details
Genetic Blueprint

Your complete lifestyle genetics profile across 16 categories: drug metabolism, methylation, neurotransmitters, caffeine response, sleep & circadian rhythm, fitness & exercise response, nutrition & metabolism, …

$29.99 View Details
Carrier Screen

Clinical-grade carrier screening powered by the ClinVar database (341,000+ variants). Identifies pathogenic variants, carrier status for recessive conditions, drug response variants, and protective variants. Includes …

$19.99 View Details
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Frequently Asked Questions

Upload your raw DNA data file from any major testing service: 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, Living DNA, or VCF files from whole genome sequencing providers like Nebula Genomics or Dante Labs. Most files are 15-40 MB. ZIP and GZIP compressed files are automatically extracted.

Most reports are ready within 5-10 minutes. Complex analyses like the Complete Genome Report may take up to 15 minutes as we scan against multiple databases.

Absolutely. Your raw genome file is deleted immediately after processing (within 1 hour). We never store, share, or sell your genetic information. Generated reports are available for download for 365 days.

No. DecodeGenome provides educational genetic analysis based on published research and clinical databases. Our reports are informational and should not replace professional medical advice.

We use three databases: our curated SNP database (79 lifestyle-relevant variants), ClinVar (NIH's 341,000+ clinical variant database), and PharmGKB (pharmacogenomic drug-gene interactions).

We support raw data from all major DNA testing services: 23andMe (all versions), AncestryDNA, MyHeritage DNA, FamilyTreeDNA, Living DNA, and VCF files from whole genome sequencing providers. Our parser auto-detects your file format — just upload and we handle the rest.

Carrier screening identifies whether you carry pathogenic gene variants for recessive conditions. Being a carrier usually means you're unaffected but could pass the variant to children.

If your report has errors or your file could not be processed, contact support@decodegenome.com and we will either re-run your analysis or provide a full refund. We stand behind the quality of our analysis.

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