Variant: rs11077627 

    present in Gene: SLC39A11
    present in Chromosome: 17
    Position on Chromosome: 72682115
    Alleles of this Variant: C/G;T

rs11077627 in SLC39A11 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.