Variant: rs10203995 

    present in Gene: ARHGEF33;LOC105374471
    present in Chromosome: 2
    Position on Chromosome: 38937913
    Alleles of this Variant: C/T

rs10203995 in ARHGEF33;LOC105374471 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.