Variant: rs199476134 

    present in Gene: ND4L;ND4;ATP6;COX3;ND3
    present in Chromosome: MT
    Position on Chromosome: 9101
    Alleles of this Variant: T/C

rs199476134 in ND4L;ND4;ATP6;COX3;ND3 gene and Optic Atrophy, Hereditary, Leber PMID 7726182 1995 A mitochondrial mutation at nt 9101 in the ATP synthase 6 gene associated with deficient oxidative phosphorylation in a family with Leber hereditary optic neuroretinopathy.