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.
PCLO · rs376091074
See detailed info → SensitiveLINC00457 · rs182139416
See detailed info → SensitiveMAFTRR · rs17689159
See detailed info → Sensitivenear LINC01648 · rs548955976
See detailed info → Sensitivenear GPR26 · rs187196172
See detailed info → SensitiveDHX16 · rs140943109
See detailed info → Sensitivenear RNASET2 · rs434093
See detailed info → SensitiveHLA · rs7768644
See detailed info → Sensitivenear VANGL2 · rs117201373
See detailed info → SensitiveTSHR · rs4903961
See detailed info → SensitiveVHRT · rs11065783
See detailed info → SensitiveHLA · rs9263688
See detailed info → SensitiveHLA-DRB6 · rs35923382
See detailed info → SensitiveHLA-DPA1 · rs4345439
See detailed info → SensitiveFBXL19 · rs8050588
See detailed info → SensitivePVT1 · rs6470578
See detailed info → SensitiveLPP · rs6780858
See detailed info → Sensitivenear VANGL2 · rs12026490
See detailed info → SensitiveCTLA4 · rs231779
See detailed info → SensitiveTNRC18 · rs748670681
See detailed info →Showing 20 of 63 · page 2 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.