Variant: rs11250778 

    present in Gene: LOC105376345
    present in Chromosome: 10
    Position on Chromosome: 1771048
    Alleles of this Variant: T/C

rs11250778 in LOC105376345 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.