Variant: rs11138852 

    present in Gene: LOC107987084
    present in Chromosome: 9
    Position on Chromosome: 80795859
    Alleles of this Variant: G/A

rs11138852 in LOC107987084 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.