237 positions on this site are linked to Medication Use as a Genetic Trait, out of 19,265 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
SLC4A7 · rs591668
See detailed info → StandardGATA4 · rs17153559
See detailed info → StandardRNY1P8 · rs12428857
See detailed info → StandardC20orf203 · rs1407256
See detailed info → StandardCHMP1A · rs154656
See detailed info → StandardRP11-347H15.4 · rs80257854
See detailed info → StandardRP11-61O1.1 · rs1257926
See detailed info → StandardCCDC88B · rs479777
See detailed info → StandardCCR8 · rs11714050
See detailed info → StandardRP11-644L4.1 · rs59183580
See detailed info → StandardRBPJ · rs7441808
See detailed info → StandardHLA-DQB1 · rs2856698
See detailed info → StandardTICAM1 · rs7254729
See detailed info → StandardRP4-781K5.8 · rs570530
See detailed info → StandardMIR31HG · rs970987
See detailed info → StandardY_RNA · rs13090803
See detailed info → StandardAC012065.4 · rs57853403
See detailed info → StandardPLEKHG1 · rs17080089
See detailed info → StandardCACNB2 · rs976785
See detailed info → StandardC10orf107 · rs72831344
See detailed info →Showing 20 of 237 · page 1 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.