63 positions on this site are linked to Graves' Disease, out of 117,958 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
RAPGEF2 · rs74461205
See detailed info → SensitiveCTNNA3 · rs72791568
See detailed info → SensitiveSYNDIG1 · rs186257749
See detailed info → Sensitivenear HLA-C · rs1639109
See detailed info → SensitiveRBMS2 · rs189834788
See detailed info → SensitiveUBAC2 · rs9557181
See detailed info → Sensitivenear TCF7 · rs57918439
See detailed info → SensitiveSEC24A · rs150348050
See detailed info → Sensitivenear HLA-B · rs9265428
See detailed info → SensitiveB3GALT4 · rs759916207
See detailed info → SensitiveRAD51B · rs74435447
See detailed info → SensitiveFAM227B · rs73398264
See detailed info → SensitiveZNF280D · rs28678122
See detailed info → SensitiveCLEC16A · rs556852922
See detailed info → Sensitivenear FBXL19 · rs7185007
See detailed info → Sensitivenear MAF · rs7190187
See detailed info → SensitiveCPD · rs183787323
See detailed info → SensitiveBCAS3 · rs145936372
See detailed info → SensitiveCTD-2378E21.1 · rs12451295
See detailed info → SensitiveTSHR · rs12101261
See detailed info →Showing 20 of 63 · page 3 of 4
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.