Variant: rs11222631 

    present in Gene: NTM
    present in Chromosome: 11
    Position on Chromosome: 131456474
    Alleles of this Variant: A/T

rs11222631 in NTM 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.