113,825 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.
near HLA-B · rs34907473
See detailed info → StandardHLA-B · rs147412087
See detailed info → Standard on its ownnear HLA-B · rs9265727
See detailed info → Standardnear HLA-B · rs114259589
See detailed info → Standard on its ownnear HLA-B · rs9265942
See detailed info → Sensitivenear HLA-B · rs6929134
See detailed info → StandardHLA-B · rs3819288
See detailed info → StandardHLA-B · rs2596487
See detailed info → StandardHLA-B · rs57989216
See detailed info → Standard on its ownnear HLA-B · rs35726795
See detailed info → Standard on its ownnear HLA-B · rs72502570
See detailed info → SensitiveHLA-B · rs2523584
See detailed info → Standardnear HLA-B · rs1634777
See detailed info → Standard on its ownnear HLA-B · rs1634769
See detailed info → Standardnear HLA-B · rs9405068
See detailed info → StandardHLA-B · rs116812356
See detailed info → Sensitivenear HLA-B · rs9391845
See detailed info → Standard on its ownnear HLA-B · rs12173764
See detailed info → Standard on its ownnear HLA-B · rs112985609
See detailed info → StandardHLA-B · rs2250293
See detailed info →Showing 20 of 167 · page 2 of 9
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.