Variant: rs10418932 

    present in Gene: C19orf47
    present in Chromosome: 19
    Position on Chromosome: 40294381
    Alleles of this Variant: T/C

rs10418932 in C19orf47 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.