Variant: rs7736962 

    present in Gene: HNRNPA1P13
    present in Chromosome: 5
    Position on Chromosome: 136429234
    Alleles of this Variant: A/C;T

rs7736962 in HNRNPA1P13 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.