Variant: rs1107573 

    present in Gene: LOC105376622
    present in Chromosome: 11
    Position on Chromosome: 34434661
    Alleles of this Variant: C/T

rs1107573 in LOC105376622 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.