Variant: rs11074738 

    present in Gene: HS3ST4
    present in Chromosome: 16
    Position on Chromosome: 25986122
    Alleles of this Variant: C/G

rs11074738 in HS3ST4 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.