Variant: rs2094787 

    present in Gene: LOC107987053;IFNA22P
    present in Chromosome: 9
    Position on Chromosome: 21280455
    Alleles of this Variant: A/G

rs2094787 in LOC107987053;IFNA22P 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.