Variant: rs10000770 

    present in Gene: INPP4B
    present in Chromosome: 4
    Position on Chromosome: 142693109
    Alleles of this Variant: C/T

rs10000770 in INPP4B 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.