rs4947296, None

N. diseases: 5
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
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
0.800 GeneticVariation GWASDB Genome-wide association study identifies GIMAP as a novel susceptibility locus for Behcet's disease. 23041938 2013
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
0.800 GeneticVariation GWASDB Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997 2012
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
0.800 GeneticVariation GWASCAT Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study. 23001997 2012
Thyrotoxic periodic paralysis
CUI: C0268446
Disease: Thyrotoxic periodic paralysis
0.700 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
Cardiomyopathy, Dilated
CUI: C0007193
Disease: Cardiomyopathy, Dilated
0.700 GeneticVariation GWASDB A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy. 23853074 2014
Meniere Disease
CUI: C0025281
Disease: Meniere Disease
0.010 GeneticVariation BEFREE We have identified the first locus, at 6p21.33, suggesting an association with bilateral MD [meta-analysis leading signal rs4947296, OR = 2.089 (1.661-2.627); <i>p</i> = 1.39 × 10<sup>-09</sup>]. 29326686 2017