Variant: rs10509309 

    present in Gene: SRGN
    present in Chromosome: 10
    Position on Chromosome: 69067525
    Alleles of this Variant: T/C

rs10509309 in SRGN 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.