8,790 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.
NOS1AP · rs17457880
See detailed info → StandardFUT1 · rs838142
See detailed info → StandardFBXL20 · rs2338796
See detailed info → StandardHLA-DQA1 · rs7744020
See detailed info → Standardnear HLA-DQB1 · rs17212223
See detailed info → StandardIRS1 · rs2972146
See detailed info → StandardCUBN · rs141640975
See detailed info → StandardCOL4A4 · rs35483183
See detailed info → StandardCUBN · rs144360241
See detailed info → Standard on its ownBACE2 · rs6517656
See detailed info → StandardAQP7 · rs144994089
See detailed info → StandardADO · rs10995311
See detailed info → StandardSBF2 · rs17368443
See detailed info → StandardERGIC3 · rs2277862
See detailed info → Standard on its ownSUPV3L1 · rs4746822
See detailed info → Standard on its ownLOC100131805 · rs7771911
See detailed info → SensitiveMAP3K8 · rs1042058
See detailed info → StandardGNA12 · rs798489
See detailed info → SensitiveBACH2 · rs1847472
See detailed info → SensitivePHACTR2 · rs12199775
See detailed info →Showing 20 of 8790 · page 324 of 440
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.