rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
|
11133798 |
2001 |
rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.
|
9452107 |
1998 |
rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.
|
10447650 |
1999 |
rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
|
8854108 |
1996 |
rs199476104
|
|
Optic Atrophy, Hereditary, Leber
|
C |
0.810 |
CausalMutation
|
CLINVAR |
Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation.
|
8470982 |
1993 |
rs199476105
|
|
Optic Atrophy, Hereditary, Leber
|
A |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
G |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
|
8854108 |
1996 |
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.
|
10447650 |
1999 |
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
|
11133798 |
2001 |
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.
|
9452107 |
1998 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
G |
0.810 |
CausalMutation
|
CLINVAR |
|
|
|
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.
|
9452107 |
1998 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic results obtained in a family with a new point mutation at nucleotide position 14498 in the ND 6 gene.
|
8854108 |
1996 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy.
|
11133798 |
2001 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.810 |
GeneticVariation
|
UNIPROT |
Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.
|
10447650 |
1999 |
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
A |
0.810 |
CausalMutation
|
CLINVAR |
|
|
|
rs200336777
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.700 |
GeneticVariation
|
UNIPROT |
|
|
|
rs28359178
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Mitochondrial DNA complex I and III mutations associated with Leber's hereditary optic neuropathy.
|
1732158 |
1992 |
rs28359178
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.700 |
GeneticVariation
|
UNIPROT |
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.
|
1900003 |
1991 |
rs28359178
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.700 |
GeneticVariation
|
UNIPROT |
The role of the ND5 gene in LHON: characterization of a new, heteroplasmic LHON mutation.
|
16240359 |
2005 |
rs28359178
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.700 |
GeneticVariation
|
UNIPROT |
When does bilateral optic atrophy become Leber hereditary optic neuropathy?
|
8213825 |
1993 |