7,216 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.
TMEM182 · rs13390641
See detailed info → StandardITCH · rs62212171
See detailed info → Standardnear BBX · rs75701938
See detailed info → StandardTLR1 · rs4833095
See detailed info → Standard on its ownPRDM11 · rs2863171
See detailed info → Standard on its ownBMP6 · rs6923462
See detailed info → Standard on its ownEFEMP1 · rs1430193
See detailed info → Standard on its ownLOC643723 · rs1159268
See detailed info → StandardBACH2 · rs10944479
See detailed info → StandardCLEC16A · rs62026376
See detailed info → StandardZBTB10 · rs7009110
See detailed info → StandardSMAD3 · rs17294280
See detailed info → StandardIL33 · rs72699186
See detailed info → StandardTSLP · rs1837253
See detailed info → StandardIL1RL1 · rs10197862
See detailed info → StandardWDR36 · rs1438673
See detailed info → StandardG6PC2 · rs3755157
See detailed info → Standardnear CREB3L1 · rs12283653
See detailed info → StandardNOS1 · rs3741475
See detailed info → StandardTAOK3 · rs6490177
See detailed info →Showing 20 of 7216 · page 263 of 361
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.