8,712 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.
LINC01515 · rs7072338
See detailed info → Standard on its ownPIK3C2B · rs12092943
See detailed info → Standard on its ownLOC644172 · rs186806998
See detailed info → Standard on its ownNCOR2 · rs11057793
See detailed info → Standard on its ownSEMA6D · rs1529883
See detailed info → Standard on its ownANO6/ARID2 · rs719700
See detailed info → Standard on its ownHTR2A · rs1410656
See detailed info → Standard on its ownnear HLA-DQB1 · rs3134986
See detailed info → Standard on its ownMC4R · rs7231880
See detailed info → Standard on its ownLRFN2 · rs6904571
See detailed info → Standard on its ownGTPBP1 · rs5750673
See detailed info → Standard on its ownGC · rs1526692
See detailed info → Standard on its ownROBO2 · rs1523766
See detailed info → Standard on its ownZFP64 · rs2206929
See detailed info → Standard on its ownnear RTL1 · rs61992671
See detailed info → Standard on its ownKDM2B · rs181617194
See detailed info → Standard on its ownAUTS2 · rs115131074
See detailed info → Standard on its ownJARID2 · rs2237149
See detailed info → Standard on its ownHLA-DQA1 · rs73728611
See detailed info → Standard on its ownHLA-DRB5 · rs117108573
See detailed info →Showing 20 of 8712 · page 20 of 436
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.