12,469 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.
GLDN · rs2446422
See detailed info → SensitiveNKX2-1 · rs944289
See detailed info → StandardSCN10A · rs6800541
See detailed info → StandardSCN5A · rs11708996
See detailed info → StandardBCL11A · rs2540917
See detailed info → StandardTFR2 · rs7786877
See detailed info → StandardHBS1L · rs4895441
See detailed info → StandardSLC17A3 · rs1408272
See detailed info → StandardHBS1L · rs7776054
See detailed info → StandardITFG3 · rs1122794
See detailed info → StandardTRAFD1 · rs11065987
See detailed info → StandardHBS1L · rs9483788
See detailed info → StandardLRP5 · rs3736228
See detailed info → StandardHLA-DQA2 · rs2858884
See detailed info → StandardNKX2-5 · rs251253
See detailed info → Standard on its ownTRHR · rs7832552
See detailed info → SensitiveKCNJ11 · rs5215
See detailed info → StandardTRIM66 · rs4929923
See detailed info → StandardNR4A2 · rs17188434
See detailed info → StandardVGLL3 · rs7642134
See detailed info →Showing 20 of 12469 · page 581 of 624
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.