63 positions on this site are linked to Graves' Disease, out of 117,874 published in total. Each was published only after passing the same quality gate; being on this list is an association, not a diagnosis.
AHI1-DT · rs9385726
See detailed info → SensitiveLINC02980 · rs775179965
See detailed info → Sensitivenear C12orf42 · rs2374049
See detailed info → SensitiveTRAF1 · rs7021880
See detailed info → SensitiveHPCAL1 · rs61671894
See detailed info → SensitiveMAGT1 · rs4826198
See detailed info → SensitiveCLEC2A · rs142468628
See detailed info → Sensitivenear CXCR4 · rs78087444
See detailed info → Sensitivenear RPL10A · rs146783471
See detailed info → Sensitivenear CTAGE13P · rs567604605
See detailed info → SensitiveTIAM1 · rs186318962
See detailed info → SensitiveHLA-DRB1*08:03 · rs116869525
See detailed info → SensitiveLINGO2 · rs73439357
See detailed info → Sensitivenear BRDT · rs374005375
See detailed info → Sensitivenear IFNGR1 · rs7759040
See detailed info → SensitivePATJ · rs369574882
See detailed info → SensitivePCAT1 · rs2466028
See detailed info → SensitiveRPS10-NUDT3 · rs193135027
See detailed info → Sensitivenear ANKS1A · rs138820558
See detailed info → SensitiveRP1 · rs573463009
See detailed info →Showing 20 of 63 · page 1 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.