8,459 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.
COX18 · rs1894292
See detailed info → SensitiveG6PD · rs1050828
See detailed info → Standard on its ownKCNJ2 · rs4793501
See detailed info → Standard on its ownXIRP1 · rs4453791
See detailed info → StandardITFG3 · rs13339636
See detailed info → StandardPRKCE · rs13008603
See detailed info → Standard on its ownTMEM16A · rs7127129
See detailed info → Standard on its ownUSP3 · rs2649
See detailed info → Standard on its ownFGGY · rs11207426
See detailed info → StandardCOBLL1 · rs13389219
See detailed info → StandardTKTL1 · rs762516
See detailed info → Standard on its ownCFDP1 · rs17696696
See detailed info → StandardFTO · rs11075990
See detailed info → StandardMC4R · rs8089364
See detailed info → Standard on its ownPALMD · rs6702619
See detailed info → Standard on its ownNFATC2 · rs6021270
See detailed info → Standard on its ownPLCL1 · rs10497813
See detailed info → Standard on its ownADAD1 · rs17388568
See detailed info → Standard on its ownDAB2 · rs7720838
See detailed info → StandardHOTTIP · rs2023844
See detailed info →Showing 20 of 8459 · page 311 of 423
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.