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.
A2ML1 · rs4883201
See detailed info → StandardNUP160 · rs747782
See detailed info → SensitiveTMPRSS2 · rs1041449
See detailed info → StandardDSTYK · rs11579220
See detailed info → StandardRUFY4 · rs144670711
See detailed info → StandardCAMK2D · rs6858698
See detailed info → StandardIL1R1 · rs13019803
See detailed info → StandardIL1RL1 · rs11693697
See detailed info → StandardIL1RL1 · rs13029918
See detailed info → StandardSLC9A4 · rs1014286
See detailed info → StandardIL1RL1 · rs17639215
See detailed info → StandardIL18RAP · rs11465699
See detailed info → StandardIL1RL1 · rs12999542
See detailed info → StandardIL1RL2 · rs2302612
See detailed info → StandardABCA1 · rs9282541
See detailed info → Standard on its ownSPPL2C · rs17690703
See detailed info → StandardNLRC5 · rs1532624
See detailed info → StandardIKZF1 · rs6583437
See detailed info → StandardLIPC · rs1077835
See detailed info → Standard on its ownPDE4D · rs159497
See detailed info →Showing 20 of 12426 · page 538 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.