Variant: rs1680684 

    present in Gene: EGLN3
    present in Chromosome: 14
    Position on Chromosome: 33954981
    Alleles of this Variant: C/T

rs1680684 in EGLN3 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.