237 positions on this site are linked to Medication Use as a Genetic Trait, out of 19,347 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
PSMC3 · rs3781627
See detailed info → StandardAFF1 · rs366327
See detailed info → StandardRP11-514O12.4 · rs71571466
See detailed info → StandardPQLC2 · rs2473808
See detailed info → StandardMED7 · rs13360007
See detailed info → StandardKIAA1524 · rs2969903
See detailed info → SensitiveIGF2BP2 · rs9854769
See detailed info → SensitiveAC007386.4 · rs2723063
See detailed info → SensitivePAM · rs116782923
See detailed info → StandardPLGRKT · rs7028486
See detailed info → StandardAC053545.3 · rs6833591
See detailed info → StandardNFATC1 · rs7240256
See detailed info → StandardBHLHE40 · rs13076468
See detailed info → StandardELMO1 · rs10279209
See detailed info → StandardCD226 · rs56249713
See detailed info → StandardTMEM131 · rs5865
See detailed info → SensitiveAC006458.3 · rs1974619
See detailed info → SensitiveGRP · rs9957264
See detailed info → StandardPLEKHA1 · rs7088058
See detailed info → SensitiveHLA-DQB1 · rs9273364
See detailed info →Showing 20 of 237 · page 11 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.