Variant: rs1769628 

    present in Gene: LOC107987210;EGLN3
    present in Chromosome: 14
    Position on Chromosome: 33965427
    Alleles of this Variant: T/A

rs1769628 in LOC107987210;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.