rs6457617, None

N. diseases: 11
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
0.800 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
0.800 GeneticVariation GWASCAT A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011
Graves Disease
CUI: C0018213
Disease: Graves Disease
0.800 GeneticVariation GWASDB A genome-wide association study identifies two new risk loci for Graves' disease. 21841780 2011