Variant: rs3176813 

    present in Gene: CCL19
    present in Chromosome: 9
    Position on Chromosome: 34690814
    Alleles of this Variant: C/T

rs3176813 in CCL19 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.