Disease: Graves Disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.120 GeneticVariation disease GWASCAT Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. 26151496 2015
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.120 GeneticVariation disease GWASDB Identification of independent risk loci for Graves' disease within the MHC in the Japanese population. 21900946 2011
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.120 GeneticVariation disease BEFREE These data reveal that the single-site polymorphism of the TAP2 gene at codon 665 may be an indicator for predicting GD development. 16721835 2006
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.120 GeneticVariation disease LHGDN These data reveal that the single-site polymorphism of the TAP2 gene at codon 665 may be an indicator for predicting GD development. 16721835 2006
CUI: C0018213
Disease: Graves Disease
Graves Disease 		0.120 GeneticVariation disease BEFREE TAP1*0301 (Val-333/Asp-637: 71% vs. 55% in controls, p < 0.008, RR = 2.05) and TAP2*0101 (Val-379/Ala-565/Thr-665/stop-687: 83% vs. 69% in controls, p < 0.03, RR = 2.20) showed a positive association with Graves' disease whereas TAP1*0401 a negative (Ile-333/Gly-637: 4% vs. 13% in controls, p < 0.01, RR = 0.25). 9027960 1997