Variant: rs6992383 

    present in Gene: LOC102723635;CCN4
    present in Chromosome: 8
    Position on Chromosome: 133211521
    Alleles of this Variant: C/T

rs6992383 in LOC102723635;CCN4 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.