Variant: rs4980201 

    present in Gene: LOC105378532
    present in Chromosome: 10
    Position on Chromosome: 123704055
    Alleles of this Variant: C/T

rs4980201 in LOC105378532 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.