Variant: rs11777682 

    present in Gene: LOC105375743;LINC00964
    present in Chromosome: 8
    Position on Chromosome: 124848154
    Alleles of this Variant: G/C

rs11777682 in LOC105375743;LINC00964 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.