9,424 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.
H2BC5 · rs1059490
See detailed info → Standard on its ownnear MAN2A1 · rs1074462
See detailed info → Standard on its ownFBXL17 · rs34410
See detailed info → Standard on its ownKCNN2 · rs3104222
See detailed info → Standard on its ownnear EFNA5 · rs35748495
See detailed info → Standard on its ownnear EFNA5 · rs7724655
See detailed info → Standard on its ownDPP4 · rs2268894
See detailed info → Standard on its ownRAPGEF4 · rs3769312
See detailed info → Standard on its ownCNTNAP5 · rs10496632
See detailed info → Standard on its ownnear SATB2 · rs71424213
See detailed info → Standard on its ownnear RBM43 · rs6705511
See detailed info → Standard on its ownGALNT13 · rs1850751
See detailed info → Standard on its ownnear RALB · rs13019313
See detailed info → Standard on its ownWDPCP · rs76262922
See detailed info → Standard on its ownnear LGALSL · rs76729733
See detailed info → Standard on its ownSTUM · rs41314284
See detailed info → Standard on its ownGATAD2B · rs4595397
See detailed info → Standard on its ownnear PLEKHO1 · rs55802315
See detailed info → Standard on its ownCADM3 · rs2253837
See detailed info → Standard on its ownFAM78B · rs4262520
See detailed info →Showing 20 of 9424 · page 7 of 472
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.