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.
FERMT3 · rs3802932
See detailed info → StandardARHGAP15 · rs76217384
See detailed info → StandardBCAS3 · rs11079428
See detailed info → StandardMECOM · rs77463690
See detailed info → StandardEBF2 · rs73563812
See detailed info → StandardCACNB2 · rs12413195
See detailed info → StandardRP5-884M6.1 · rs35301188
See detailed info → StandardUHRF1 · rs2656918
See detailed info → StandardAC005592.2 · rs7716114
See detailed info → StandardMSRA · rs7460226
See detailed info → StandardPLCE1 · rs2901761
See detailed info → StandardCELSR2 · rs4970834
See detailed info → StandardCACNB2 · rs7070847
See detailed info → StandardCNNM2 · rs79668541
See detailed info → StandardGOSR2 · rs11874
See detailed info → StandardMYBPC3 · rs2856653
See detailed info → StandardGUCY1A3 · rs56329057
See detailed info → StandardCTC-573M9.1 · rs11743404
See detailed info → StandardPLCB1 · rs6039216
See detailed info → StandardRP4-663N10.1 · rs146754848
See detailed info →Showing 20 of 237 · page 5 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.