GenoLens — Genomic Intelligence
at Your Fingertips
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.
Everything you need, in one tooltip
Four query types, fifteen data sources, zero context-switching.
Gene Lookup
Instantly retrieve HGNC nomenclature, PanelApp diagnostic grades, ClinGen validity, and MANE transcripts.
Variant Analysis
ClinVar pathogenicity, gnomAD frequencies, VEP functional predictions, and AlphaMissense AI scores in one view.
Disease Associations
Open Targets association scores, DDG2P developmental disorders, and Orphanet rare disease links.
Literature Search
LitVar2 variant-specific papers and Europe PMC disease literature, ranked by relevance.
Powered by 15 trusted sources
Curated databases used by clinical geneticists and researchers worldwide.
How it works
Three steps to clinical-grade annotations.
Highlight or type
Select any gene symbol, variant (rsID or HGVS), HPO term, or disease name on a page — or type it into the toolbar popup.
Instant tooltip
A compact panel appears beside your selection with tabbed, multi-source annotations.
Clinical insights
Review pathogenicity, population frequency, disease associations, and literature — all in context.
Follow the trail
Click a linked gene, disease, or phenotype to look it up next, and step back through where you've been.
Free forever. Pro when you need more.
Every lookup above is free and unlimited, with no account. Pro adds the interpretation layer on top.
Free
$0 · no account required
Unlimited lookups across all 15 public databases, the Variant Evidence Strength Score, cancer evidence from CIViC and Cancer Hotspots, and AlphaFold structure thumbnails.
Pro
$9.99/month · cancel anytime
- AI Variant Interpretation reports
- AI Cancer Tier reports (AMP/ASCO/CAP)
- Trial Watch — weekly new clinical-trial alerts
- Pro PDF audit of the Evidence Strength Score
- Citation generator (BibTeX / RIS / APA)
- Unlimited saved queries & favorites
For Research Use Only. AI reports summarise public-database evidence and are not clinical recommendations.
Ready to accelerate your research?
Join researchers who save hours every week with instant genomic annotations.