rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
G |
0.810 |
CausalMutation
|
CLINVAR |
|
|
|
rs199476108
|
|
Optic Atrophy, Hereditary, Leber
|
A |
0.810 |
CausalMutation
|
CLINVAR |
|
|
|
rs397515506
|
|
Optic Atrophy, Hereditary, Leber
|
T |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
rs387906425
|
|
Optic Atrophy, Hereditary, Leber
|
A |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
rs199476106
|
|
Optic Atrophy, Hereditary, Leber
|
G |
0.800 |
CausalMutation
|
CLINVAR |
|
|
|
rs387906424
|
|
Optic Atrophy, Hereditary, Leber
|
T |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs200336777
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.700 |
GeneticVariation
|
UNIPROT |
|
|
|
rs199476105
|
|
Optic Atrophy, Hereditary, Leber
|
A |
0.700 |
CausalMutation
|
CLINVAR |
|
|
|
rs387906425
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.800 |
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 |
Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy.
|
1900003 |
1991 |
rs199476108
|
|
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 |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs397515506
|
|
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 |
An ND-6 mitochondrial DNA mutation associated with Leber hereditary optic neuropathy.
|
1417830 |
1992 |
rs869025186
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.700 |
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 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 in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.
|
9452107 |
1998 |
rs397515506
|
|
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 |
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 |
rs869025186
|
|
Optic Atrophy, Hereditary, Leber
|
|
0.700 |
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
|
C |
0.810 |
CausalMutation
|
CLINVAR |
Leber's hereditary optic neuropathy. Clinical manifestations of the 14484 mutation.
|
8470982 |
1993 |
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 |
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 |
rs397515506
|
|
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 |
Leber's hereditary optic neuropathy: clinical and molecular genetic findings in a patient with a new mutation in the ND6 gene.
|
10447650 |
1999 |