Variant: rs1156668 

    present in Gene: LINC01705
    present in Chromosome: 1
    Position on Chromosome: 222032466
    Alleles of this Variant: A/C;T

rs1156668 in LINC01705 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.