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.
B3GALTL · rs9542236
See detailed info → StandardSLC16A8 · rs8135665
See detailed info → StandardDARC · rs2340727
See detailed info → StandardLIPC · rs920915
See detailed info → StandardCETP · rs1864163
See detailed info → StandardORM1 · rs10982156
See detailed info → StandardENOX1 · rs9533425
See detailed info → StandardFLJ33360 · rs12518614
See detailed info → StandardCFHR4 · rs10922162
See detailed info → StandardF7/F10 · rs3211770
See detailed info → StandardF13A1 · rs1318606
See detailed info → StandardF7/F10 · rs555212
See detailed info → StandardFCER1A · rs16827466
See detailed info → StandardHLA-DRB5 · rs4530903
See detailed info → Standard on its ownSPRY2 · rs8001641
See detailed info → Standard on its ownIL2 · rs17454584
See detailed info → Standard on its ownBCL6 · rs6773854
See detailed info → StandardCERKL · rs1449263
See detailed info → StandardOR2K2 · rs10980800
See detailed info → StandardHLA-DQA2 · rs7764819
See detailed info →Showing 20 of 8459 · page 343 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.