8,408 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.
FAM13A · rs4416442
See detailed info → Standard on its ownSIAE · rs12282107
See detailed info → Standard on its ownALMS1 · rs11884776
See detailed info → Standard on its ownACSM2B · rs7499271
See detailed info → Standard on its ownACADL · rs1509569
See detailed info → Standard on its ownACY3 · rs12288023
See detailed info → Standard on its ownGATM · rs2433610
See detailed info → SensitiveTGFB2 · rs4846480
See detailed info → Standard on its ownSLC6A13 · rs555044
See detailed info → SensitiveCOX18 · rs1894292
See detailed info → SensitiveG6PD · rs1050828
See detailed info → Standard on its ownKCNJ2 · rs4793501
See detailed info → Standard on its ownXIRP1 · rs4453791
See detailed info → StandardITFG3 · rs13339636
See detailed info → StandardPRKCE · rs13008603
See detailed info → Standard on its ownTMEM16A · rs7127129
See detailed info → Standard on its ownUSP3 · rs2649
See detailed info → Standard on its ownFGGY · rs11207426
See detailed info → StandardCOBLL1 · rs13389219
See detailed info → StandardTKTL1 · rs762516
See detailed info →Showing 20 of 8408 · page 308 of 421
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.