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.
APOB · rs1041968
See detailed info → StandardLPA · rs12208357
See detailed info → StandardHLA-area · rs114067101
See detailed info → StandardLIPG · rs149615216
See detailed info → StandardLCAT · rs2271293
See detailed info → SensitiveDUSP10 · rs6691170
See detailed info → StandardLIPC · rs10468017
See detailed info → StandardLRRC32 · rs7130588
See detailed info → SensitiveITGAM · rs11574637
See detailed info → StandardLEF1 · rs2650000
See detailed info → StandardACAN · rs2351491
See detailed info → SensitiveTNPO3 · rs12537284
See detailed info → SensitiveLPL · rs2083637
See detailed info → StandardWDR72 · rs17730281
See detailed info → StandardLRP1B · rs2890652
See detailed info → StandardNOS2 · rs4795067
See detailed info → StandardNFE2L3 · rs1055144
See detailed info → StandardNISCH · rs6784615
See detailed info → SensitiveTMEM129 · rs798766
See detailed info → StandardBCAS3 · rs11868441
See detailed info →Showing 20 of 12469 · page 573 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.