Highlight any gene or variant on a webpage to instantly see clinical annotations from 15 trusted databases. No tab-switching, no copy-paste — just select and know.
Four query types, fifteen data sources, zero context-switching.
Instantly retrieve HGNC nomenclature, PanelApp diagnostic grades, ClinGen validity, and MANE transcripts.
ClinVar pathogenicity, gnomAD frequencies, VEP functional predictions, and AlphaMissense AI scores in one view.
Open Targets association scores, DDG2P developmental disorders, and Orphanet rare disease links.
LitVar2 variant-specific papers and Europe PMC disease literature, ranked by relevance.
Curated databases used by clinical geneticists and researchers worldwide.
Three steps to clinical-grade annotations.
Select any gene symbol, variant ID, HPO term, or disease name on any webpage.
A compact panel appears beside your selection with tabbed, multi-source annotations.
Review pathogenicity, population frequency, disease associations, and literature — all in context.
Join researchers who save hours every week with instant genomic annotations.
