12,505 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.
HLA-DRB1 · rs115231074
See detailed info → StandardLRRC37B · rs17780086
See detailed info → Standard on its ownPON-1 · rs854572
See detailed info → SensitiveCOL27A1 · rs7868992
See detailed info → StandardF3 · rs2022309
See detailed info → StandardPRRC2A · rs1046089
See detailed info → StandardSLCO1B1 · rs11045879
See detailed info → Standard on its ownPDGFRA · rs17084051
See detailed info → StandardCCND2 · rs10849023
See detailed info → StandardMARCH8 · rs901683
See detailed info → SensitiveATP11A · rs1278769
See detailed info → StandardOR51I1 · rs7948471
See detailed info → Standard on its ownBBS9 · rs10262453
See detailed info → StandardC7orf58 · rs4609139
See detailed info → StandardAHCYL2 · rs11766298
See detailed info → StandardMTMR3 · rs12537
See detailed info → SensitiveARID5B · rs10821944
See detailed info → StandardHLA-DRB1 · rs660895
See detailed info → SensitiveNFKBIE · rs2233434
See detailed info → SensitiveCD83 · rs12529514
See detailed info →Showing 20 of 12505 · page 551 of 626
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.