Variant: rs121909602 

    present in Gene: COX6B1
    present in Chromosome: 19
    Position on Chromosome: 35651302
    Alleles of this Variant: G/A

rs121909602 in COX6B1 gene and Cytochrome-c Oxidase Deficiency PMID 18499082 2008 Severe infantile encephalomyopathy caused by a mutation in COX6B1, a nucleus-encoded subunit of cytochrome c oxidase.