Variant: rs10747750 

    present in Gene: OR6C66P
    present in Chromosome: 12
    Position on Chromosome: 55387430
    Alleles of this Variant: C/T

rs10747750 in OR6C66P 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.