7,592 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.
AQP1 · rs28362721
See detailed info → StandardRSPO3 · rs10457487
See detailed info → StandardCSNK1G3 · rs11745493
See detailed info → Standardnear CSNK1G3 · rs3905510
See detailed info → Standardnear CTNNB1 · rs447911
See detailed info → Standardnear CCDC34 · rs10450586
See detailed info → StandardAMBRA1 · rs7112229
See detailed info → Standardnear ZNF408 · rs11606709
See detailed info → StandardDGKZ · rs34406563
See detailed info → StandardSOX6 · rs3809095
See detailed info → Standardnear ZBTB40 · rs10493013
See detailed info → StandardSPATS2 · rs1270901
See detailed info → StandardFMN2 · rs12044944
See detailed info → Standardnear EN1 · rs144832051
See detailed info → StandardSLC30A10 · rs185048405
See detailed info → Standardnear AKAP11 · rs9594738
See detailed info → StandardSOX6 · rs35199438
See detailed info → StandardSOX6 · rs12800049
See detailed info → StandardTUBA1C · rs117557198
See detailed info → StandardDDB2 · rs4647728
See detailed info →Showing 20 of 7592 · page 38 of 380
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.