8,284 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.
PAX3 · rs7559271
See detailed info → StandardSP3 · rs4325816
See detailed info → StandardDYM · rs1787200
See detailed info → StandardARSE · rs12393627
See detailed info → Standard on its ownRUNX3 · rs11249215
See detailed info → StandardCOBLL1 · rs12328675
See detailed info → StandardIDOL · rs3757354
See detailed info → Standard on its ownSCARB1 · rs11057841
See detailed info → StandardHPR · rs2000999
See detailed info → Standard on its ownRTEL1 · rs4809324
See detailed info → StandardMAP3K3 · rs11658329
See detailed info → Standardnear CSH1 · rs2854160
See detailed info → Standard on its ownMLLT10 · rs11012732
See detailed info → StandardHLA-C · rs10484554
See detailed info → StandardSLC22A2 · rs3127573
See detailed info → StandardITGA4 · rs12988934
See detailed info → StandardADAM19 · rs2277027
See detailed info → Standard on its ownACADL · rs2286963
See detailed info → Standard on its ownDAB2IP · rs7025486
See detailed info → StandardRIPK2 · rs42490
See detailed info →Showing 20 of 8284 · page 345 of 415
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.