Variant: rs17118854 

    present in Gene: HSD52;LINC01358
    present in Chromosome: 1
    Position on Chromosome: 59139460
    Alleles of this Variant: A/C

rs17118854 in HSD52;LINC01358 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.