Variant: rs10110509 

    present in Gene: NUGGC
    present in Chromosome: 8
    Position on Chromosome: 28076881
    Alleles of this Variant: G/A

rs10110509 in NUGGC 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.