Variant: rs16861634 

    present in Gene: CP
    present in Chromosome: 3
    Position on Chromosome: 149213737
    Alleles of this Variant: G/A;T

rs16861634 in CP 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.