rs1131691575
|
|
0.925 |
0.080 |
15 |
89317469 |
missense variant
|
C/T
|
snv
|
8.0E-06
|
1.4E-05
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs121918048
|
|
0.882 |
0.200 |
15 |
89320953 |
missense variant
|
G/A
|
snv
|
|
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs121918053
|
|
1.000 |
|
15 |
89321777 |
missense variant
|
G/A
|
snv
|
1.2E-05
|
2.8E-05
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs121918056
|
|
0.882 |
0.080 |
15 |
89330257 |
missense variant
|
G/A
|
snv
|
4.0E-06
|
7.0E-06
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs145843073
|
|
0.882 |
0.080 |
15 |
89327198 |
missense variant
|
T/C
|
snv
|
4.7E-04
|
6.3E-04
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs2307440
|
|
1.000 |
|
15 |
89318587 |
missense variant
|
G/A
|
snv
|
1.9E-04
|
1.5E-04
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs556925652
|
|
1.000 |
|
15 |
89325664 |
missense variant
|
G/A
|
snv
|
2.0E-05
|
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs61752784
|
|
1.000 |
|
15 |
89330133 |
missense variant
|
C/G
|
snv
|
3.4E-03
|
3.6E-03
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs753410045
|
|
1.000 |
|
15 |
89318710 |
missense variant
|
C/G;T
|
snv
|
2.0E-05
|
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs763393580
|
|
1.000 |
|
15 |
89321194 |
missense variant
|
C/T
|
snv
|
4.0E-05
|
2.1E-05
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs781168350
|
|
1.000 |
|
15 |
89326639 |
missense variant
|
C/T
|
snv
|
4.0E-06
|
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
1.000 |
14 |
2001 |
2006 |
rs121918052
|
|
1.000 |
0.160 |
15 |
89327006 |
missense variant
|
C/G;T
|
snv
|
1.3E-04;
8.0E-06
|
|
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
|
0.700 |
1.000 |
10 |
2003 |
2016 |
rs61752783
|
|
0.882 |
0.200 |
15 |
89326947 |
missense variant
|
C/A;G
|
snv
|
4.8E-03;
2.0E-05
|
|
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
|
0.700 |
1.000 |
9 |
2003 |
2006 |
rs769827124
|
|
0.882 |
0.200 |
15 |
89322749 |
missense variant
|
G/A
|
snv
|
2.4E-05
|
1.4E-05
|
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
|
0.700 |
1.000 |
9 |
2003 |
2006 |
rs41549716
|
|
0.882 |
0.200 |
15 |
89321842 |
missense variant
|
T/C
|
snv
|
6.6E-03
|
7.0E-03
|
Alpers Syndrome (disorder)
|
0.700 |
1.000 |
7 |
2004 |
2014 |
rs41549716
|
|
0.882 |
0.200 |
15 |
89321842 |
missense variant
|
T/C
|
snv
|
6.6E-03
|
7.0E-03
|
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1
|
0.700 |
1.000 |
7 |
2002 |
2008 |
rs776031396
|
|
1.000 |
0.160 |
15 |
89317492 |
stop gained
|
G/A;T
|
snv
|
8.0E-06
|
|
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1
|
0.700 |
1.000 |
7 |
2002 |
2008 |
rs113994093
|
|
1.000 |
0.120 |
15 |
89330241 |
missense variant
|
C/T
|
snv
|
1.2E-05
|
1.4E-05
|
Leigh Disease
|
0.700 |
1.000 |
1 |
2009 |
2009 |
rs113994098
|
|
0.742 |
0.320 |
15 |
89321792 |
missense variant
|
C/T
|
snv
|
1.5E-04
|
2.7E-04
|
Leigh Disease
|
0.700 |
1.000 |
1 |
2009 |
2009 |
rs1010372555
|
|
1.000 |
|
15 |
89318712 |
missense variant
|
G/A;C
|
snv
|
4.0E-06;
4.0E-06
|
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
|
0 |
|
|
rs11546842
|
|
0.925 |
0.200 |
15 |
89320890 |
missense variant
|
G/A
|
snv
|
2.4E-05
|
1.1E-04
|
Progressive External Ophthalmoplegia with Mitochondrial DNA Deletions, Autosomal Dominant, 1
|
0.700 |
|
0 |
|
|
rs375305567
|
|
0.925 |
0.200 |
15 |
89325519 |
missense variant
|
C/T
|
snv
|
3.2E-05
|
7.7E-05
|
Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
|
0.700 |
|
0 |
|
|
rs56047213
|
|
1.000 |
0.080 |
15 |
89318617 |
missense variant
|
C/T
|
snv
|
|
7.0E-06
|
Alpers Syndrome (disorder)
|
0.700 |
|
0 |
|
|
rs745539599
|
|
1.000 |
|
15 |
89329042 |
missense variant
|
C/A
|
snv
|
4.0E-06
|
7.0E-06
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
|
0 |
|
|
rs768028281
|
|
1.000 |
|
15 |
89319064 |
missense variant
|
C/T
|
snv
|
8.0E-06
|
7.0E-06
|
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA WITH MITOCHONDRIAL DNA DELETIONS, AUTOSOMAL RECESSIVE 1
|
0.700 |
|
0 |
|
|