8,909 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.
HLA-C · rs17197839
See detailed info → SensitiveCELF2 · rs35202367
See detailed info → SensitiveMYO15A · rs854807
See detailed info → SensitiveSBNO2 · rs11669443
See detailed info → SensitiveLPP · rs11719821
See detailed info → SensitiveBNC2 · rs10962474
See detailed info → SensitiveSOD1 · rs13048019
See detailed info → SensitiveBCAS4 · rs62202837
See detailed info → SensitiveSMC2 · rs7859034
See detailed info → SensitiveAC017060.1 · rs17137933
See detailed info → SensitiveEXOC2 · rs9392026
See detailed info → SensitiveLINC01248 · rs2882274
See detailed info → SensitiveCFL1 · rs10896064
See detailed info → SensitiveAC010745.4 · rs6739779
See detailed info → SensitiveRP4-799G3.2 · rs12070203
See detailed info → SensitiveLOC105755953 · rs74623270
See detailed info → StandardDNAJB12 · rs9416017
See detailed info → StandardTMEM161B-AS1 · rs7737179
See detailed info → StandardTHRB · rs4260345
See detailed info → StandardPDE3A · rs7971334
See detailed info →Showing 20 of 8909 · page 13 of 446
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.