Variant: rs4857741 

    present in Gene: LINC00578;LOC101928711
    present in Chromosome: 3
    Position on Chromosome: 177766177
    Alleles of this Variant: A/G

rs4857741 in LINC00578;LOC101928711 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.