237 positions on this site are linked to Medication Use as a Genetic Trait, out of 19,354 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
PLCB1 · rs6039216
See detailed info → StandardZBTB46 · rs8118848
See detailed info → StandardCTSO · rs62328145
See detailed info → StandardRAC1 · rs78745308
See detailed info → StandardRP13-487K5.1 · rs4691666
See detailed info → StandardU2 · rs2984644
See detailed info → StandardCTD-2507G9.1 · rs56175671
See detailed info → StandardRP11-664H17.1 · rs7952935
See detailed info → StandardTRIM49B · rs10839204
See detailed info → StandardITPKA · rs1757463
See detailed info → StandardCSK · rs11072508
See detailed info → StandardZNF831 · rs6026739
See detailed info → StandardNPBWR2 · rs6122248
See detailed info → StandardGATA4 · rs11250157
See detailed info → StandardKDM6B · rs62059712
See detailed info → StandardTFAP2B · rs3857599
See detailed info → StandardAC016735.1 · rs115262049
See detailed info → StandardLINC00322 · rs76346476
See detailed info → StandardAP001046.5 · rs762395
See detailed info → StandardTBC1D19 · rs28667801
See detailed info →Showing 20 of 237 · page 6 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.