12,469 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.
near CTH · rs2651244
See detailed info → Sensitivenear ZBTB40 · rs12568930
See detailed info → SensitiveFOS · rs4899554
See detailed info → StandardKCNV2 · rs10738760
See detailed info → StandardMGC45491 · rs9472155
See detailed info → StandardZFPM2 · rs6993770
See detailed info → StandardMRPL14 · rs4513773
See detailed info → StandardUGT1A1 · rs6742078
See detailed info → StandardRREB1 · rs6931262
See detailed info → StandardSPTBN1 · rs11898505
See detailed info → StandardCELSR2 · rs12740374
See detailed info → SensitiveCD40 · rs1569723
See detailed info → SensitiveKIR2DL1 · rs11672983
See detailed info → SensitiveRPS6KB1 · rs1292053
See detailed info → SensitiveCEBPB · rs913678
See detailed info → Standard on its ownFTO · rs12149832
See detailed info → StandardPCSK1 · rs261967
See detailed info → StandardCDKAL1 · rs9356744
See detailed info → SensitiveSCARB2 · rs6812193
See detailed info → SensitiveEXOC2 · rs12210050
See detailed info →Showing 20 of 12469 · page 579 of 624
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.