Variant: rs17201248 

    present in Gene: SNHG32;SNORD48;SNORD52
    present in Chromosome: 6
    Position on Chromosome: 31835353
    Alleles of this Variant: C/G;T

rs17201248 in SNHG32;SNORD48;SNORD52 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.

rs17201248 in SNHG32;SNORD48;SNORD52 gene and Graves Disease PMID 26151496 2015 Genetic determinants of antithyroid drug-induced agranulocytosis by human leukocyte antigen genotyping and genome-wide association study.