Variant: rs4396773 

    present in Gene: NFATC2;LOC105372663
    present in Chromosome: 20
    Position on Chromosome: 51392255
    Alleles of this Variant: C/T

rs4396773 in NFATC2;LOC105372663 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.