12,426 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.
EEFSEC · rs2999052
See detailed info → StandardHAAO · rs3816183
See detailed info → StandardPKDCC · rs988958
See detailed info → Standard on its ownCAPN14 · rs149864795
See detailed info → SensitiveURAD · rs9581943
See detailed info → StandardCAV1 · rs10258482
See detailed info → StandardSLC2A9 · rs80204783
See detailed info → StandardMAP4K2 · rs10897526
See detailed info → Standardnear ZNF518B · rs79824542
See detailed info → StandardZNF518B · rs34208161
See detailed info → SensitivePTHLH · rs10771399
See detailed info → Standard on its ownMPO · rs12940923
See detailed info → StandardSLC2A9 · rs116142041
See detailed info → Standard on its ownC17orf71 · rs6503905
See detailed info → StandardMNS1 · rs11636802
See detailed info → StandardACOXL · rs17483466
See detailed info → SensitiveCDCA7 · rs4972593
See detailed info → StandardADCY9 · rs879620
See detailed info → StandardARL15 · rs3776717
See detailed info → StandardINHBC · rs3741414
See detailed info →Showing 20 of 12426 · page 513 of 622
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.