12,423 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.
PLG · rs4252129
See detailed info → StandardSHROOM3 · rs10032549
See detailed info → StandardKLK3 · rs2659051
See detailed info → StandardSLC41A1 · rs6679073
See detailed info → Standard on its ownC6orf204 · rs6906287
See detailed info → Standard on its ownCDKN1A · rs1321313
See detailed info → StandardGLT25D2 · rs3814333
See detailed info → StandardGSDMB · rs2305480
See detailed info → SensitiveTOX3 · rs12922061
See detailed info → SensitiveFAF1 · rs17106184
See detailed info → SensitiveTMEM154 · rs6813195
See detailed info → Standard on its ownEDN1 · rs5370
See detailed info → Standard on its ownF12 · rs2731672
See detailed info → StandardNRG4 · rs11072566
See detailed info → StandardC3orf47 · rs6439167
See detailed info → StandardIGF2BP3 · rs12534093
See detailed info → StandardOR2J3 · rs3129109
See detailed info → Standard on its ownIGHG1 · rs10136766
See detailed info → SensitiveLILRA3 · rs103294
See detailed info → StandardPEPD · rs4805885
See detailed info →Showing 20 of 12423 · page 527 of 622
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.