237 positions on this site are linked to Medication Use as a Genetic Trait, out of 19,389 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
RBMS3 · rs1968514
See detailed info → StandardSLC25A46 · rs10055042
See detailed info → StandardC11orf30 · rs11236797
See detailed info → StandardSLC15A5 · rs10846305
See detailed info → StandardBOK-AS1 · rs7567892
See detailed info → StandardBTNL2 · rs9268500
See detailed info → StandardGNG12-AS1 · rs17130567
See detailed info → StandardLDLR · rs73015016
See detailed info → StandardMEPE · rs899040
See detailed info → StandardCDKN2B-AS1 · rs1831733
See detailed info → StandardRP11-396O20.2 · rs10832519
See detailed info → StandardENPEP · rs7685862
See detailed info → StandardKDM2B · rs60370741
See detailed info → StandardPRDM6 · rs1422278
See detailed info → StandardZFP91 · rs10896795
See detailed info → StandardCMIP · rs7203816
See detailed info → StandardFBN2 · rs6595839
See detailed info → StandardPLCB1 · rs4813867
See detailed info → StandardMIR4513 · rs2168518
See detailed info → StandardTAGLN · rs494356
See detailed info →Showing 20 of 237 · page 8 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.