Variant: rs207459999

present in Gene: CYTB;ND6 present in Chromosome: MT Position on Chromosome: 15242 Alleles of this Variant: G/A

rs207459999 in CYTB;ND6 gene and Leigh Disease PMID 11047755 2000 Mitochondrial encephalomyopathy and complex III deficiency associated with a stop-codon mutation in the cytochrome b gene.