Variant: rs168569 

    present in Gene: TMEM161B
    present in Chromosome: 5
    Position on Chromosome: 88190721
    Alleles of this Variant: T/C

rs168569 in TMEM161B 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.