Variant: rs2192636 

    present in Gene: LOC101927026;LINC01195
    present in Chromosome: 16
    Position on Chromosome: 9455007
    Alleles of this Variant: C/T

rs2192636 in LOC101927026;LINC01195 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.