Variant: rs12979895 

    present in Gene: LOC100507373
    present in Chromosome: 19
    Position on Chromosome: 14142214
    Alleles of this Variant: C/A

rs12979895 in LOC100507373 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.