12,425 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.
UGT1A1 · rs11563251
See detailed info → Standard on its ownKCNJ2 · rs6501431
See detailed info → Standard on its ownGPATCH1 · rs10416265
See detailed info → SensitiveCCR6 · rs1854853
See detailed info → Standard on its ownESR1 · rs2982552
See detailed info → StandardDAGLB · rs702485
See detailed info → StandardIGF2BP1 · rs1994969
See detailed info → StandardCACNB2 · rs10740993
See detailed info → SensitiveSLC26A9 · rs4077468
See detailed info → StandardAJUBA · rs997154
See detailed info → Standardnear CEBPA · rs10401672
See detailed info → StandardCALU · rs1799922
See detailed info → SensitiveTET2 · rs9790517
See detailed info → SensitiveITPR1 · rs6762644
See detailed info → StandardLPAR1 · rs1007000
See detailed info → StandardCHSY1 · rs752092
See detailed info → StandardTJP1 · rs785422
See detailed info → StandardFOXO1 · rs2721051
See detailed info → SensitiveDIRC3 · rs16857609
See detailed info → SensitiveMETAP1D · rs2016394
See detailed info →Showing 20 of 12425 · page 521 of 622
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.