Variant: rs1075457 

    present in Gene: SEPTIN9
    present in Chromosome: 17
    Position on Chromosome: 77404655
    Alleles of this Variant: C/T

rs1075457 in SEPTIN9 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.