8,759 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.
IL12B · rs4379175
See detailed info → Standard on its ownCHRNA5 · rs17486278
See detailed info → Standard on its ownMMP12 · rs17368659
See detailed info → StandardCYP2A6 · rs56113850
See detailed info → Standard on its ownMYO1D · rs379123
See detailed info → Standard on its ownAGPHD1 · rs11852372
See detailed info → Standard on its ownKCNJ2 · rs6501431
See detailed info → SensitiveTBC1D21 · rs16958445
See detailed info → StandardCRYAA · rs11911275
See detailed info → Standardnear GRM3 · rs274632
See detailed info → Standard on its ownCPS1 · rs1047891
See detailed info → StandardUGT1A1 · rs11563251
See detailed info → Standardnear CSMD1 · rs2407746
See detailed info → Standardnear PRAG1 · rs2921036
See detailed info → SensitiveTLE4 · rs17791513
See detailed info → StandardABCG2 · rs4148152
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 →Showing 20 of 8759 · page 337 of 438
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.