Variant: rs1131692063 

    present in Gene: CYTB;ND5
    present in Chromosome: MT
    Position on Chromosome: 13051
    Alleles of this Variant: G/A

rs1131692063 in CYTB;ND5 gene and Optic Atrophy, Hereditary, Leber PMID 27164671 2016 The m.13051G>A mitochondrial DNA mutation results in variable neurology and activated mitophagy.

PMID 12736867 2003 Sequence analysis of the mitochondrial genomes from Dutch pedigrees with Leber hereditary optic neuropathy.