Variant: rs199476115 

    present in Gene: COX1;ND2
    present in Chromosome: MT
    Position on Chromosome: 5244
    Alleles of this Variant: G/A

rs199476115 in COX1;ND2 gene and Optic Atrophy, Hereditary, Leber PMID 1732158 1992 Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.

PMID 1900003 1991 Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.