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.
PLEKHG1 · rs17080089
See detailed info → StandardWNT2B · rs72993045
See detailed info → StandardNQO1 · rs2917677
See detailed info → StandardSETD2 · rs34850939
See detailed info → StandardLRPPRC · rs10183431
See detailed info → StandardACVRL1 · rs2293093
See detailed info → StandardRP1-292L20.1 · rs221907
See detailed info → StandardRP1-167A14.2 · rs1951459
See detailed info → StandardRP11-542C16.2 · rs35776863
See detailed info → StandardLPP · rs12634152
See detailed info → StandardIRF4 · rs9391997
See detailed info → StandardTM6SF2 · rs187429064
See detailed info → StandardTRPS1 · rs2737245
See detailed info → StandardAC022431.2 · rs11743303
See detailed info → StandardSMARCA4 · rs73013176
See detailed info → StandardPVRL2 · rs79701229
See detailed info → StandardBCL7C · rs11864054
See detailed info → StandardPVRL2 · rs41289512
See detailed info → StandardAC068138.1 · rs10804330
See detailed info → StandardBSND · rs12739394
See detailed info →Showing 20 of 237 · page 2 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.