9,424 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.
KCNJ5 · rs76097649
See detailed info → StandardREEP3 · rs12245149
See detailed info → StandardFBXO32 · rs62521286
See detailed info → StandardGATA4 · rs35620480
See detailed info → StandardOPN1SW · rs55985730
See detailed info → StandardUST · rs117984853
See detailed info → StandardHSF2 · rs13195459
See detailed info → StandardCDKN1A · rs3176326
See detailed info → StandardNR3C1 · rs6580277
See detailed info → StandardWNT8A · rs2040862
See detailed info → StandardCAMK2D · rs6829664
See detailed info → StandardFGF5 · rs1458038
See detailed info → StandardGNB4 · rs7612445
See detailed info → StandardSCN10A · rs6790396
See detailed info → StandardCAND2 · rs7650482
See detailed info → StandardERBB4 · rs35544454
See detailed info → StandardSPATS2L · rs3820888
See detailed info → StandardGYPC · rs28387148
See detailed info → StandardUSP34 · rs11125871
See detailed info → StandardKIF3C · rs7578393
See detailed info →Showing 20 of 9424 · page 462 of 472
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.