9,718 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-DQB · rs241428
See detailed info → StandardIL1F10 · rs6734238
See detailed info → StandardBCL7B · rs13233571
See detailed info → StandardAPOE · rs4420638
See detailed info → SensitiveTNFAIP3 · rs10499194
See detailed info → Standard on its ownCPS1 · rs7422339
See detailed info → SensitivePSCA · rs2294008
See detailed info → SensitiveIL6ST · rs10065637
See detailed info → StandardPRKCE · rs10495928
See detailed info → Standard on its ownMYH6 · rs365990
See detailed info → StandardLMX1B · rs2275241
See detailed info → StandardDERA · rs151326733
See detailed info → StandardTXNRD2 · rs73148965
See detailed info → StandardPDE7B · rs9494457
See detailed info → StandardLOC107986141 · rs11710139
See detailed info → StandardMECOM · rs73174345
See detailed info → StandardMYOF · rs61861119
See detailed info → StandardANGPT1 · rs10505100
See detailed info → StandardTHSD7A · rs12699251
See detailed info → StandardARHGEF12 · rs58073046
See detailed info →Showing 20 of 9718 · page 469 of 486
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.