Variant: rs12462498 

    present in Gene: CRTC1
    present in Chromosome: 19
    Position on Chromosome: 18722140
    Alleles of this Variant: C/T

rs12462498 in CRTC1 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.