rs199476104
|
0.925 |
0.160 |
MT |
14484 |
missense variant |
T/C
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.810 |
1.000 |
7 |
1992 |
2001 |
rs199476108
|
1.000 |
0.160 |
MT |
14482 |
missense variant |
C/A;G
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.810 |
1.000 |
6 |
1992 |
2002 |
rs199476106
|
1.000 |
0.160 |
MT |
14495 |
missense variant |
A/G
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.800 |
1.000 |
5 |
1992 |
2001 |
rs397515506
|
1.000 |
0.160 |
MT |
14568 |
missense variant |
C/T
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.800 |
1.000 |
5 |
1992 |
2001 |
rs387906425
|
1.000 |
0.160 |
MT |
13730 |
missense variant |
G/A
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.800 |
1.000 |
4 |
1991 |
2005 |
rs869025186
|
1.000 |
0.160 |
MT |
14498 |
missense variant |
T/C
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.700 |
1.000 |
5 |
1992 |
2001 |
rs28359178
|
0.882 |
0.280 |
MT |
13708 |
missense variant |
G/A
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.700 |
1.000 |
4 |
1991 |
2005 |
rs41518645
|
0.925 |
0.200 |
MT |
15257 |
missense variant |
G/A
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
1992 |
1992 |
rs199476105
|
0.851 |
0.200 |
MT |
14459 |
missense variant |
G/A
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs200336777
|
1.000 |
0.160 |
MT |
15812 |
missense variant |
G/A
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs387906424
|
0.925 |
0.200 |
MT |
14596 |
missense variant |
A/T
|
snv
|
|
|
Optic Atrophy, Hereditary, Leber
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Eye Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|