Variant: rs2075580 

    present in Gene: DDX39B;ATP6V1G2-DDX39B;SNORD117
    present in Chromosome: 6
    Position on Chromosome: 31536198
    Alleles of this Variant: G/A;C

rs2075580 in DDX39B;ATP6V1G2-DDX39B;SNORD117 gene and Graves Disease PMID 21900946 2011 Identification of independent risk loci for Graves' disease within the MHC in the Japanese population.