Variant: rs10963072 

    present in Gene: CNTLN
    present in Chromosome: 9
    Position on Chromosome: 17378778
    Alleles of this Variant: G/A;C;T

rs10963072 in CNTLN 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.