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.
ZFAND6 · rs11634397
See detailed info → StandardCILP2 · rs2304130
See detailed info → StandardHBS1L · rs7775698
See detailed info → SensitiveIGF2BP2 · rs6769511
See detailed info → SensitiveZNF365 · rs10995190
See detailed info → SensitiveTMEM175 · rs113881148
See detailed info → Sensitivenear ANKRD50 · rs13147255
See detailed info → SensitiveHLA-DQA2 · rs3997848
See detailed info → SensitiveHLA-DQA2 · rs35122968
See detailed info → SensitiveMNDA · rs857786
See detailed info → SensitiveLINC01149 · rs9501130
See detailed info → SensitivePSORS1C3 · rs116763857
See detailed info → SensitiveHLA-A · rs34941730
See detailed info → SensitiveTNFAIP3 · rs12665429
See detailed info → SensitiveICOSLG · rs56178904
See detailed info → SensitiveMAPT · rs1052553
See detailed info → SensitiveAKAP11 · rs74537115
See detailed info → SensitiveITGB7 · rs7313065
See detailed info → SensitiveM6PR · rs1805731
See detailed info → SensitiveFLI1 · rs605093
See detailed info →Showing 20 of 12444 · page 593 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.