What this does

• Type an rsID, gene symbol, or chr:pos to see your genotype and SnpEff/ClinVar annotations.
• Type a phenotype (e.g. Alzheimer's disease, type 2 diabetes, warfarin sensitivity) to see which literature-linked variants you actually carry.
• The interpretation agent ranks findings by materiality and cites published sources.

Nothing here is diagnostic. Any material finding needs clinical-grade confirmation and a genetic counsellor.