Variant: rs959996 

    present in Gene: LOC105372663;NFATC2
    present in Chromosome: 20
    Position on Chromosome: 51392872
    Alleles of this Variant: G/A;C

rs959996 in LOC105372663;NFATC2 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.