rs199476119
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.
|
1928099 |
1991 |
rs199476119
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy.
|
1674640 |
1991 |
rs199476119
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs199476119
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.
|
1900003 |
1991 |
rs199476119
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation.
|
2018041 |
1991 |
rs199476119
|
|
C |
0.800 |
CausalMutation |
CLINVAR |
|
|
|
rs199476119
|
|
|
0.800 |
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 |
rs1599988
|
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs28616230
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Mitochondrial DNA C4171A/ND1 is a novel primary causative mutation of Leber's hereditary optic neuropathy with a good prognosis.
|
12112111 |
2002 |
rs28616230
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Association of the mtDNA m.4171C>A/MT-ND1 mutation with both optic neuropathy and bilateral brainstem lesions.
|
24884847 |
2014 |
rs28616230
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Rare primary mitochondrial DNA mutations and probable synergistic variants in Leber's hereditary optic neuropathy.
|
22879922 |
2012 |
rs28616230
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Novel A14841G mutation is associated with high penetrance of LHON/C4171A family.
|
19555656 |
2009 |
rs28616230
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs28616230
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Sequence variation in mitochondrial complex I genes: mutation or polymorphism?
|
15972314 |
2006 |
rs199476118
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy.
|
1674640 |
1991 |
rs199476118
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs199476118
|
|
A |
0.810 |
CausalMutation |
CLINVAR |
Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.
|
1928099 |
1991 |
rs199476118
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Leber hereditary optic neuropathy: involvement of the mitochondrial ND1 gene and evidence for an intragenic suppressor mutation.
|
2018041 |
1991 |
rs199476118
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.
|
1928099 |
1991 |
rs199476118
|
|
|
0.810 |
GeneticVariation |
UNIPROT |
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.
|
1900003 |
1991 |
rs199476118
|
|
|
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 |
rs41460449
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
Leber hereditary optic neuropathy: identification of the same mitochondrial ND1 mutation in six pedigrees.
|
1928099 |
1991 |
rs41460449
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
A new mtDNA mutation associated with Leber hereditary optic neuroretinopathy.
|
1674640 |
1991 |
rs41460449
|
|
|
0.800 |
GeneticVariation |
UNIPROT |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs41460449
|
|
|
0.800 |
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 |