Variant: rs4736441 

    present in Gene: CCN4;LOC102723635
    present in Chromosome: 8
    Position on Chromosome: 133212326
    Alleles of this Variant: G/A;C

rs4736441 in CCN4;LOC102723635 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.