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.
near HLA-DQA1 · rs116352702
See detailed info → SensitiveHLA-DQA1 · rs140780894
See detailed info → Sensitivenear HLA-DQA2 · rs9275599
See detailed info → SensitiveHIP1 · rs118048475
See detailed info → SensitiveSLC15A4 · rs10847697
See detailed info → SensitiveBLK · rs2736346
See detailed info → SensitiveIRF5 · rs4731532
See detailed info → SensitiveFLNB · rs4076852
See detailed info → SensitiveTNIP1 · rs3792783
See detailed info → SensitiveIRF5 · rs36073657
See detailed info → SensitiveFLG2 · rs76285340
See detailed info → SensitiveIGHM · rs45471499
See detailed info → Standardnear PEX5 · rs7973719
See detailed info → Standard on its ownCD30L · rs7853287
See detailed info → StandardADIPOQ · rs10937273
See detailed info → Standard on its ownDDAH1 · rs28489187
See detailed info → StandardAADAT · rs11726248
See detailed info → StandardPRDM11 · rs17723470
See detailed info → StandardCAPZB · rs10799824
See detailed info → StandardVEGFA · rs9472138
See detailed info →Showing 20 of 12426 · page 499 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.