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Sample Analysis Results

Real results from a whole genome sequencing analysis of ~4 million variants. This is what your dashboard will look like after uploading your genetic data.

Analyze your own genome

Run Date

Mar 15, 2026

File Format

.vcf.gz

Chip / Platform

wgs

Variants Read

3,962,722

Genome Build

GRCh37

Pipeline Runtime

122.2s

Curated SNPs

Found 245 out of 247 important SNPs.

View all SNP results →

Pharmacogenomics

74 genes analyzed

View pharmacogenomics results →

ClinVar Annotations

2,472 of your variants have ClinVar annotations

View ClinVar annotations →

Polygenic Risk ScoresExperimental

17 polygenic risk scores computed

View PRS results →

Analyze Your Own Genome

Upload your 23andMe, AncestryDNA, or whole genome sequencing (VCF) file to get a comprehensive analysis like this one. Your raw genetic data is never stored.

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