Variant: rs1680679 

    present in Gene: EGLN3;LOC107987210
    present in Chromosome: 14
    Position on Chromosome: 33965501
    Alleles of this Variant: G/A

rs1680679 in EGLN3;LOC107987210 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.