Variant: rs10117017 

    present in Gene: SNX30
    present in Chromosome: 9
    Position on Chromosome: 112811301
    Alleles of this Variant: G/C

rs10117017 in SNX30 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.