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.
RP11-542A14.1 · rs7701003
See detailed info → StandardTCF21 · rs162185
See detailed info → StandardMAPKAP1 · rs1250505
See detailed info → StandardSTAT6 · rs3001426
See detailed info → StandardRXFP2 · rs7983337
See detailed info → StandardNAT2 · rs73207888
See detailed info → StandardLMAN1L · rs34862454
See detailed info → StandardHLA-DRB1 · rs687308
See detailed info → SensitiveRP11-73O6.4 · rs719728
See detailed info → SensitivePABPC4 · rs2293476
See detailed info → SensitiveTCF7L2 · rs61123794
See detailed info → SensitiveAGBL2 · rs1056387
See detailed info → StandardRP11-428L9.2 · rs1775553
See detailed info → StandardU6 · rs2102418
See detailed info → StandardFAM105A · rs74455974
See detailed info → StandardSLC25A46 · rs7735519
See detailed info → StandardIL2 · rs56293330
See detailed info → StandardRPS26 · rs34415530
See detailed info → StandardRANGAP1 · rs139496
See detailed info → StandardHLA-DQA1 · rs17843580
See detailed info →Showing 20 of 237 · page 10 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.