Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs199476112
rs199476112
ND4 ; ND5
0.810 GeneticVariation UNIPROT Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations. 9452107

1998

dbSNP: rs199476112
rs199476112
ND4 ; ND5
0.810 GeneticVariation UNIPROT Electron transfer properties of NADH:ubiquinone reductase in the ND13460 and the ND411778 mutations of the Leber hereditary optic neuroretinopathy (LHON). 1959619

1991

dbSNP: rs199476112
rs199476112
ND4 ; ND5
0.810 GeneticVariation UNIPROT Detection of the G to A mitochondrial DNA mutation at position 11778 in German families with Leber's hereditary optic neuropathy. 1959931

1991

dbSNP: rs199476112
rs199476112
ND4 ; ND5
0.810 GeneticVariation UNIPROT Mitochondrial DNA mutation associated with Leber's hereditary optic neuropathy. 3201231

1988

dbSNP: rs200613617
rs200613617
COX3 ; ND3 ; ND4 ; ND4L
0.800 GeneticVariation UNIPROT

dbSNP: rs199476134
rs199476134
ATP6 ; COX3 ; ND3 ; ND4 ; ND4L
0.700 GeneticVariation UNIPROT 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. 7726182

1995

dbSNP: rs193302933
rs193302933
ND3 ; ND4 ; ND4L ; ND5
0.700 GeneticVariation UNIPROT

dbSNP: rs267606611
rs267606611
ATP6 ; COX3 ; ND3 ; ND4 ; ND4L
0.700 GeneticVariation UNIPROT