Variant: rs10500896 

    present in Gene: NELL1
    present in Chromosome: 11
    Position on Chromosome: 21169470
    Alleles of this Variant: C/T

rs10500896 in NELL1 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.