Variant: rs1123479

present in Gene: LOC105372663 present in Chromosome: 20 Position on Chromosome: 51379774 Alleles of this Variant: T/C

rs1123479 in LOC105372663 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.