Variant: rs387906425 

    present in Gene: CYTB;ND6;ND5
    present in Chromosome: MT
    Position on Chromosome: 13730
    Alleles of this Variant: G/A

rs387906425 in CYTB;ND6;ND5 gene and Optic Atrophy, Hereditary, Leber PMID 1900003 1991 Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.

PMID 1732158 1992 Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.

PMID 8213825 1993 When does bilateral optic atrophy become Leber hereditary optic neuropathy?

PMID 16240359 2005 The role of the ND5 gene in LHON: characterization of a new, heteroplasmic LHON mutation.