237 positions on this site are linked to Medication Use as a Genetic Trait, out of 19,328 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
ASGR1 · rs72837687
See detailed info → StandardCOG5 · rs4515482
See detailed info → StandardSOX6 · rs11023910
See detailed info → StandardNCALD · rs513159
See detailed info → StandardRP11-819C21.1 · rs664485
See detailed info → StandardCMIP · rs62043959
See detailed info → StandardCTD-2140G10.1 · rs11026578
See detailed info → StandardRP11-101C11.1 · rs112339942
See detailed info → StandardPGPEP1 · rs12459368
See detailed info → StandardAC012361.1 · rs73228424
See detailed info → StandardRXFP2 · rs1200385
See detailed info → StandardFES · rs1894401
See detailed info → StandardRP11-73O6.4 · rs9375459
See detailed info → StandardOR4A15 · rs11229252
See detailed info → StandardFBN2 · rs17677603
See detailed info → StandardRP1-158P9.1 · rs778124
See detailed info → StandardOR2K2 · rs113537788
See detailed info → StandardCLCN6 · rs2050265
See detailed info → StandardRP11-73O6.4 · rs62436821
See detailed info → StandardC10orf107 · rs17210692
See detailed info →Showing 20 of 237 · page 3 of 12
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.