Variant: rs1017527 

    present in Gene: INPP4B;LOC101927613
    present in Chromosome: 4
    Position on Chromosome: 142661771
    Alleles of this Variant: T/C

rs1017527 in INPP4B;LOC101927613 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.