Variant: rs11189600 

    present in Gene: HPS1
    present in Chromosome: 10
    Position on Chromosome: 98419517
    Alleles of this Variant: C/A;T

rs11189600 in HPS1 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.

rs11189600 in HPS1 gene and Serum albumin measurement PMID 23281178 2013 A genome-wide assessment of variability in human serum metabolism.