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.
ELOVL7 · rs62372074
See detailed info → StandardIGSF11 · rs62264764
See detailed info → StandardDPP4 · rs6432708
See detailed info → StandardTTC29 · rs3827592
See detailed info → StandardCADM2 · rs1549979
See detailed info → StandardNAV2 · rs35891966
See detailed info → StandardTMEM182 · rs6720941
See detailed info → StandardHEATR5A · rs61754158
See detailed info → StandardEPHA7 · rs6938042
See detailed info → StandardEPHX2 · rs1565735
See detailed info → StandardPOU3F2 · rs2132029
See detailed info → StandardOLFM1 · rs7019640
See detailed info → StandardCABP1 · rs34067374
See detailed info → StandardTPM3 · rs35761479
See detailed info → StandardPDE4B · rs2186122
See detailed info → StandardCPSF6 · rs317660
See detailed info → StandardKCNJ3 · rs2652434
See detailed info → StandardUGP2 · rs140144265
See detailed info → StandardEED · rs1466802
See detailed info → StandardDKFZp686O1327 · rs1427499
See detailed info →Showing 20 of 7519 · page 39 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.