Variant: rs16999774 

    present in Gene: LINC01858
    present in Chromosome: 19
    Position on Chromosome: 23063598
    Alleles of this Variant: G/A

rs16999774 in LINC01858 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.