10,689 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.
HBS1L · rs9373124
See detailed info → StandardLTBR-TNFRSF1A · rs11616188
See detailed info → StandardSTARD13 · rs9315204
See detailed info → StandardRPL27A · rs4929949
See detailed info → StandardIL12A · rs6441286
See detailed info → StandardMMP13 · rs74380195
See detailed info → StandardASCL4 · rs60222088
See detailed info → StandardKSR2 · rs11615756
See detailed info → StandardALG10B · rs35011311
See detailed info → StandardEMPI1 · rs2417268
See detailed info → StandardTRPC6 · rs11224896
See detailed info → StandardFADS2 · rs174541
See detailed info → StandardADO · rs224111
See detailed info → StandardTMEM38B · rs971415
See detailed info → StandardTLE4 · rs13284688
See detailed info → StandardZBTB5 · rs17502738
See detailed info → StandardDCAF12 · rs62560863
See detailed info → StandardFOCAD · rs10811438
See detailed info → Standard on its ownRFT1 · rs13088281
See detailed info → SensitiveHNF4A · rs4812829
See detailed info →Showing 20 of 10689 · page 468 of 535
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.