7,519 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.
UST · 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 → StandardHAND2 · rs4615152
See detailed info → StandardNEURL1 · rs11598047
See detailed info → StandardPRRX1 · rs577676
See detailed info → StandardKCNN3 · rs36004974
See detailed info → StandardPKP2 · rs1454934
See detailed info →Showing 20 of 7519 · page 367 of 376
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.