Variant: rs132881 

    present in Gene: LOC112267891;NUP50
    present in Chromosome: 22
    Position on Chromosome: 45171699
    Alleles of this Variant: C/A

rs132881 in LOC112267891;NUP50 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.