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.
near IRF8 · rs11117432
See detailed info → StandardIL12A · rs485499
See detailed info → StandardMHC · rs7774434
See detailed info → SensitiveHLA-DQB1 · rs2040406
See detailed info → StandardZBTB38 · rs9825379
See detailed info → StandardIGF1 · rs5742692
See detailed info → StandardTNFRSF1A · rs1800693
See detailed info → StandardADIPOQ · rs17366568
See detailed info → SensitiveSKAP1 · rs9303542
See detailed info → StandardPLAG1 · rs7833986
See detailed info → SensitiveBABAM1 · rs8170
See detailed info → StandardACADS · rs2014355
See detailed info → StandardKCNQ1 · rs12576239
See detailed info → SensitiveABO · rs505922
See detailed info → SensitiveIRF8 · rs17445836
See detailed info → StandardKCNH2 · rs2968864
See detailed info → StandardGINS3 · rs37062
See detailed info → StandardPRKAG2 · rs10224002
See detailed info → StandardHK1 · rs16926246
See detailed info → StandardC6orf182 · rs11966072
See detailed info →Showing 20 of 12469 · page 587 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.