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.
PTGER4 · rs4613763
See detailed info → SensitiveICOSLG · rs762421
See detailed info → SensitiveMUC19 · rs11175593
See detailed info → SensitiveC11orf30 · rs7927894
See detailed info → Sensitivenear TRIB1 · rs1551398
See detailed info → Sensitivenear TNFSF18 · rs9286879
See detailed info → SensitiveCCR6 · rs2301436
See detailed info → SensitiveATG16L1 · rs2241880
See detailed info → SensitiveMST1 · rs9858542
See detailed info → SensitiveKLF3 · rs6856616
See detailed info → SensitiveHLA-DRA · rs10947261
See detailed info → SensitiveSTARD10 · rs11235667
See detailed info → SensitiveSOX11 · rs11894081
See detailed info → SensitiveLOC100129633 · rs6478106
See detailed info → SensitiveHLA-DQA2 · rs7765379
See detailed info → SensitiveTBC1D1 · rs1487630
See detailed info → StandardNCAN · rs10401969
See detailed info → Standard on its ownMICA · rs4418214
See detailed info → SensitiveLAMA5 · rs4925386
See detailed info → SensitiveEIF3H · rs16892766
See detailed info →Showing 20 of 12444 · page 599 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.