Variant: rs1556423844 

    present in Gene: ND4;ND3;ND4L;ND5
    present in Chromosome: MT
    Position on Chromosome: 10663
    Alleles of this Variant: T/C

rs1556423844 in ND4;ND3;ND4L;ND5 gene and Optic Atrophy, Hereditary, Leber PMID 8680405 1995 Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations.

PMID 11935318 2002 The role of mtDNA background in disease expression: a new primary LHON mutation associated with Western Eurasian haplogroup J.