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Open Variant Registry

Variants We Analyze

Browse every genetic variant in our database. We believe in transparency — you should know exactly what we test before you upload your DNA.

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Want to see what your DNA says? Upload your existing 23andMe or AncestryDNA file.

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About Our Variant Registry

Every variant in this registry has been curated from peer-reviewed sources including ClinVar (NCBI), the GWAS Catalog (NHGRI-EBI), and PharmGKB. Evidence levels follow international standards: Level 1A represents the strongest evidence backed by clinical practice guidelines, while Level 4 represents exploratory findings from preliminary studies.

Variants marked as "Physician Review Required" have clinical implications that benefit from professional interpretation. These results are shown to you immediately with clear disclaimers, and you can request a physician review for expert guidance — included with Premium + Physician and Family plans, or available per-result starting at $35.

Our variant database grows continuously through automated discovery from reference databases, followed by expert geneticist review. Each addition is tracked in an auditable change history.