Variant: rs10484435 

    present in Gene: H3C2
    present in Chromosome: 6
    Position on Chromosome: 26031583
    Alleles of this Variant: T/G

rs10484435 in H3C2 gene and Corpuscular Hemoglobin Concentration Mean PMID 23222517 2012 Seventy-five genetic loci influencing the human red blood cell.

rs10484435 in H3C2 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.