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.
HDAC9 · rs2073963
See detailed info → StandardANO6 · rs17095830
See detailed info → StandardSTARD3 · rs11869286
See detailed info → StandardGJA1 · rs9398652
See detailed info → StandardFADS1 · rs174546
See detailed info → SensitiveRBM43 · rs7560163
See detailed info → StandardHLA-DQA/B · rs1794275
See detailed info → StandardHLA-DPB1 · rs9277535
See detailed info → Standard on its ownHLA-DQB1 · rs10484561
See detailed info → Standardnear BUD13 · rs11216126
See detailed info → SensitiveATP5SL · rs11672691
See detailed info → StandardRASGRF1 · rs939658
See detailed info → Standard on its ownPBLD · rs12571093
See detailed info → StandardRANKL · rs1021188
See detailed info → StandardNADSYN1 · rs3829251
See detailed info → StandardCHEK2 · rs1547014
See detailed info → StandardHMGA1 · rs206936
See detailed info → Standard on its ownnear MICB · rs2255221
See detailed info → StandardC3 · rs3745567
See detailed info → StandardCFHR1 · rs3753394
See detailed info →Showing 20 of 12469 · page 583 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.