Variant: rs12650358 

    present in Gene: LOC101928879;LNX1
    present in Chromosome: 4
    Position on Chromosome: 53575437
    Alleles of this Variant: C/A

rs12650358 in LOC101928879;LNX1 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.