Variant: rs11777631 

    present in Gene: LINC00964;LOC105375743
    present in Chromosome: 8
    Position on Chromosome: 124847895
    Alleles of this Variant: G/A

rs11777631 in LINC00964;LOC105375743 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.