Variant: rs681059 

    present in Gene: HSH2D
    present in Chromosome: 19
    Position on Chromosome: 16158696
    Alleles of this Variant: C/G;T

rs681059 in HSH2D gene and Leukemia, Myelocytic, Acute PMID 27903959 2017 Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia.