12,444 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.
HTT · rs61348208
See detailed info → StandardNRXN3 · rs10150332
See detailed info → StandardZNF483 · rs10980926
See detailed info → StandardITPA · rs7270101
See detailed info → StandardSEC16B · rs543874
See detailed info → StandardMAP2K5 · rs2241423
See detailed info → StandardGIPR · rs2287019
See detailed info → SensitiveHLA-DQA2 · rs10947262
See detailed info → StandardLIPC · rs4775041
See detailed info → StandardBYSL · rs11970772
See detailed info → StandardFBX07 · rs9609565
See detailed info → StandardHBS1L · rs9402686
See detailed info → StandardBET1L · rs11602954
See detailed info → StandardRNF219-AS1 · rs2243517
See detailed info → Standard— · rs4275621
See detailed info → Standard— · rs1592757
See detailed info → StandardPTPRF · rs3001723
See detailed info → StandardDUSP6 · rs1427829
See detailed info → StandardSORCS3 · rs11591402
See detailed info → SensitiveCDKAL1 · rs4712524
See detailed info →Showing 20 of 12444 · page 592 of 623
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.