12,426 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-DQB · rs9275326
See detailed info → SensitiveGPNMB · rs199347
See detailed info → SensitiveINPP5F · rs117896735
See detailed info → StandardHLA-DQA1 · rs9461776
See detailed info → Standard on its ownANKRD27 · rs3815700
See detailed info → StandardSCN10A · rs6798015
See detailed info → StandardMEIS1 · rs10865355
See detailed info → SensitiveSIPA1L2 · rs10797576
See detailed info → SensitiveSTK39 · rs1474055
See detailed info → SensitiveGBA · rs35749011
See detailed info → Standard on its ownDCHS2 · rs2045323
See detailed info → Standard on its ownESR1 · rs3020331
See detailed info → StandardDLG4 · rs314253
See detailed info → Standard on its ownCCDC27 · rs1175550
See detailed info → Standard on its ownPSMB4 · rs2769264
See detailed info → StandardFTO · rs62033400
See detailed info → SensitiveBRIP1 · rs34289250
See detailed info → StandardHBS1L · rs9376090
See detailed info → Standard on its ownCYP19A1 · rs2414095
See detailed info → StandardMPP3 · rs8077889
See detailed info →Showing 20 of 12426 · page 502 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.