Variant: rs9262631

present in Gene: HCG22 present in Chromosome: 6 Position on Chromosome: 31056824 Alleles of this Variant: C/A;T

rs9262631 in HCG22 gene and Drug-induced neutropenia PMID 26151496 2015 Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study.

rs9262631 in HCG22 gene and Graves Disease PMID 26151496 2015 Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study.