Variant: rs1037153 

    present in Gene: LOC105370064
    present in Chromosome: 12
    Position on Chromosome: 127203391
    Alleles of this Variant: C/T

rs1037153 in LOC105370064 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.