8,698 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.
COPG2 · rs6971499
See detailed info → SensitiveZDHHC11 · rs2736098
See detailed info → SensitiveZFP1 · rs7190458
See detailed info → Standard on its ownPDILT · rs4494548
See detailed info → SensitiveLRRK2 · rs76904798
See detailed info → SensitiveCCDC62 · rs11060180
See detailed info → Standard on its ownDMGDH · rs705415
See detailed info → Standard on its ownARSB · rs248381
See detailed info → SensitiveINPP5F · rs117896735
See detailed info → Standard on its ownANKRD27 · rs3815700
See detailed info → SensitiveARRDC3 · rs10474352
See detailed info → StandardHLA-DQA1 · rs9461776
See detailed info → SensitiveGPNMB · rs199347
See detailed info → SensitiveHLA-DQB · rs9275326
See detailed info → SensitiveTMEM175 · rs34311866
See detailed info → SensitiveZC3H11A · rs4951011
See detailed info → Standard on its ownMEIS1 · rs10865355
See detailed info → Standard on its ownSCN10A · rs6798015
See detailed info → SensitivePRC1 · rs2290203
See detailed info → SensitiveGBA · rs35749011
See detailed info →Showing 20 of 8698 · page 315 of 435
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.