Variant: rs10138733 

    present in Gene: LOC107984685
    present in Chromosome: 14
    Position on Chromosome: 29186112
    Alleles of this Variant: A/G

rs10138733 in LOC107984685 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.