HCP5, HLA complex P5, 10866

N. diseases: 79; N. variants: 33
Disease: Graves Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs2596449
rs2596449
Entrez Id: 10866;352961
Gene Symbol: HCP5;HCG26
HCP5;HCG26
CUI: C0018213
Disease:
Graves Disease 		A 0.700 GeneticVariation GWASCAT Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study. 26151496 2015