Variant: rs4875958 

    present in Gene: CLN8
    present in Chromosome: 8
    Position on Chromosome: 1772924
    Alleles of this Variant: G/A;C

rs4875958 in CLN8 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.

rs4875958 in CLN8 gene and Systolic Pressure PMID 30224653 2018 Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits.