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.
RP11-344J7.2 · rs9472136
See detailed info → StandardAC019100.3 · rs1486195
See detailed info → StandardPTP4A3 · rs12549801
See detailed info → Standard7SK · rs62039768
See detailed info → StandardRP4-662A9.2 · rs2105092
See detailed info → StandardPPAP2B · rs61772578
See detailed info → StandardCDC25A · rs6800730
See detailed info → StandardCNTF · rs11229555
See detailed info → StandardFAT1 · rs11726072
See detailed info → StandardARPC1A · rs143524414
See detailed info → StandardPPAP2B · rs61772626
See detailed info → StandardRP4-663N10.1 · rs57748895
See detailed info → StandardSVEP1 · rs76038906
See detailed info → StandardLRPPRC · rs13387221
See detailed info → StandardSBF2 · rs12274440
See detailed info → StandardSHBG · rs12938899
See detailed info → StandardPLEKHG1 · rs62434123
See detailed info → StandardERAP1 · rs27041
See detailed info → StandardGML · rs7463212
See detailed info → StandardWDR36 · rs6594499
See detailed info →Showing 20 of 237 · page 7 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.