Variant: rs10504098 

    present in Gene: SNTG1
    present in Chromosome: 8
    Position on Chromosome: 50174661
    Alleles of this Variant: A/G

rs10504098 in SNTG1 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.