Genomic Report — Analyze Your DNA File
Upload your raw genome file from 23andMe, AncestryDNA, MyHeritage, FTDNA, or a VCF file (GRCh37/GRCh38) — including whole-genome or whole-exome sequencing (WGS/WES) VCFs up to 2 GB — and get a clinical-grade genomic analysis in minutes. The analysis runs 100% in your browser — your file never leaves your device. No file yet? A bundled demo genome unlocks the full Complete-tier report experience instantly, with no upload, signup, or payment required.
What the Report Includes
Your report covers disease risk across 1,000+ conditions using ClinVar and GWAS Catalog data, pharmacogenomics for 41 genes and 110 drug pairs following CPIC guidelines, ACMG v3.2 secondary findings across all 81 official genes including BRCA1/2 and Lynch syndrome genes, ancestry-specific founder-mutation carrier panels, and ancestry breakdown, plus trait analysis and a Lifestyle Blueprint on higher plans. Every condition and trait match can also be exported as a CSV spreadsheet. Learn about pharmacogenomics or how genomes work.
Supported File Formats
Raw genotype exports (not processed reports) from 23andMe, AncestryDNA, MyHeritage, and FTDNA, plus VCF files in GRCh37 or GRCh38 build — including whole-genome and whole-exome sequencing (WGS/WES) VCFs up to 2 GB, streamed and parsed client-side. For VCF files, biallelic SNVs and clean biallelic indels with rs-prefixed IDs are supported.
Pricing
Preview 2 body systems, 3 trait insights, and your ancestry summary for free. Full access starts at $12.99 for a one-time 30-Day Pass (no subscription), or from $9.99/month as an ongoing Essentials subscription — higher tiers (Plus, Complete) add the full Traits tab and Lifestyle Blueprint. See our science methodology or return to the home page.