Variant: rs17630699 

    present in Gene: LOC107985213
    present in Chromosome: 1
    Position on Chromosome: 158493296
    Alleles of this Variant: T/C

rs17630699 in LOC107985213 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.