8,242 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.
EN1 · rs6542457
See detailed info → Standard on its ownKRTAP · rs143290289
See detailed info → Standard on its ownHOXC13 · rs11170678
See detailed info → Standard on its ownPDE11A · rs116825096
See detailed info → Standard on its ownHECTD4 · rs144504271
See detailed info → Standard on its ownIKZF1 · rs11980379
See detailed info → StandardGCK · rs2971669
See detailed info → Standard on its ownPADI3 · rs11585357
See detailed info → Standard on its ownPLEKHA7 · rs11024074
See detailed info → Standard on its ownTMEM116 · rs7294902
See detailed info → Standard on its ownLMAN1L · rs6495122
See detailed info → Standard on its ownCACNB2 · rs11014166
See detailed info → Standardnear FAM3C · rs73719807
See detailed info → Standard on its ownMUC1 · rs4460629
See detailed info → Standardnear FUBP3 · rs10120794
See detailed info → StandardGRB10 · rs1548607
See detailed info → StandardDCDC1 · rs273573
See detailed info → Standard on its ownWNT3 · rs919462
See detailed info → Standard on its ownnear MYOCD · rs72809171
See detailed info → Standard on its ownMSI2 · rs17833789
See detailed info →Showing 20 of 8242 · page 27 of 413
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.