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.
FAM108C1 · rs7174222
See detailed info → StandardSORCS3 · rs191572726
See detailed info → StandardCACNA1D · rs9841978
See detailed info → StandardC10orf107 · rs72821787
See detailed info → StandardACE · rs4305
See detailed info → StandardAC023797.1 · rs75366683
See detailed info → StandardLPP · rs60946162
See detailed info → StandardGLIS3 · rs10814853
See detailed info → StandardNSMCE1 · rs11646066
See detailed info → StandardTSLP · rs1898671
See detailed info → StandardSLC7A10 · rs117710327
See detailed info → StandardRP11-152C17.1 · rs6802894
See detailed info → StandardIL4R · rs2239347
See detailed info → StandardFADS2 · rs174572
See detailed info → StandardIL18R1 · rs11679146
See detailed info → StandardAC004041.2 · rs115008099
See detailed info → StandardRP11-428L9.1 · rs2025758
See detailed info → StandardRORA · rs11071559
See detailed info → StandardRP11-81K2.1 · rs12952581
See detailed info → StandardCLEC16A · rs35441874
See detailed info →Showing 20 of 237 · page 9 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.