Variant: rs28359178 

    present in Gene: CYTB;ND5;ND6
    present in Chromosome: MT
    Position on Chromosome: 13708
    Alleles of this Variant: G/A

rs28359178 in CYTB;ND5;ND6 gene and Optic Atrophy, Hereditary, Leber PMID 1732158 1992 Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.

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

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

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