237 positions on this site are linked to Medication Use as a Genetic Trait, out of 19,328 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
CDKN2B-AS1 · rs7018475
See detailed info → SensitiveRN5S188 · rs145510090
See detailed info → SensitiveCDKN2B-AS1 · rs10965246
See detailed info → SensitiveHCG27 · rs1619179
See detailed info → StandardCAMSAP2 · rs12742404
See detailed info → StandardZCCHC7 · rs563132
See detailed info → StandardAZIN1 · rs2247355
See detailed info → StandardRP11-89M16.1 · rs1561924
See detailed info → StandardCEP68 · rs2252867
See detailed info → StandardTIMMDC1 · rs4688013
See detailed info → StandardRAD51B · rs3784099
See detailed info → StandardINPP5B · rs61776678
See detailed info → StandardKIAA1683 · rs11666808
See detailed info → StandardPANX1 · rs2282655
See detailed info → StandardATP6V0D1 · rs8056260
See detailed info → StandardEIF2C2 · rs7823699
See detailed info → StandardTG · rs853320
See detailed info →Showing 17 of 237 · page 12 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.