rs4947296, None

N. diseases: 5
Disease: Graves Disease ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.810 GeneticVariation GWASCAT Assessment of Molecular Subtypes in Thyrotoxic Periodic Paralysis and Graves Disease Among Chinese Han Adults: A Population-Based Genome-Wide Association Study. 31050781 2019
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.810 GeneticVariation BEFREE Ultimately, we did not confirm the reported genetic markers of early-onset GD in our Chinese Han population but found that a GD-risk SNP located in the human leukocyte antigen class I region-rs4947296-was more strongly correlated with early-onset GD than non-early-onset GD. 28598035 2018
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.810 GeneticVariation GWASCAT A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.810 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011