Variant: rs11958127 

    present in Gene: LOC105377714;LOC105377715
    present in Chromosome: 5
    Position on Chromosome: 169472802
    Alleles of this Variant: C/T

rs11958127 in LOC105377714;LOC105377715 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.