12,469 variants MyGeneLog™ checks for — each with its own plain-language page and cited source. New findings are collected from the public GWAS Catalog every twenty minutes.
TBX3 · rs11067228
See detailed info → Standard on its ownFGFR2 · rs10788160
See detailed info → SensitiveNRGN · rs12807809
See detailed info → Standard on its ownMMP · rs495366
See detailed info → StandardSOX17 · rs10958409
See detailed info → StandardPRKCE · rs10168349
See detailed info → SensitiveCLPTM1L · rs31489
See detailed info → SensitiveHLA-DRB1 · rs2647044
See detailed info → SensitiveTNFAIP3 · rs2327832
See detailed info → Sensitivenear RBPJ · rs10517086
See detailed info → SensitiveMAP3K7 · rs10806425
See detailed info → StandardCEP72 · rs924607
See detailed info → StandardCFB · rs429608
See detailed info → SensitiveTP53 · rs78378222
See detailed info → SensitiveKRT5 · rs11170164
See detailed info → SensitiveRHOU · rs801114
See detailed info → SensitiveRCC2 · rs7538876
See detailed info → StandardHLA-C · rs11575839
See detailed info → Standard on its ownKLK3 · rs17632542
See detailed info → StandardC6orf204 · rs11153730
See detailed info →Showing 20 of 12469 · page 585 of 624
One specific position in the genome (an rsID), explained in plain language with what published research has found it linked to, and how strong that link actually is.
The public GWAS Catalog, checked every twenty minutes, plus variants added manually after research review. Every one passes the same quality gate before publishing.
No. Listing reflects an association from published research, not a diagnosis or a cause. Most common variants shift probability modestly rather than determining an outcome.
Yes — the search box above matches gene symbols and rsIDs as well as trait names.