Variant: rs3761055 

    present in Gene: MAP1S
    present in Chromosome: 19
    Position on Chromosome: 17725022
    Alleles of this Variant: T/C;G

rs3761055 in MAP1S 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.