rs886041014
|
1.000 |
0.120 |
19 |
6495531 |
missense variant |
A/C
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs886041022
|
1.000 |
0.120 |
19 |
6495318 |
missense variant |
A/C
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs886041020
|
1.000 |
0.120 |
19 |
6495336 |
missense variant |
A/G
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs886041018
|
1.000 |
0.120 |
19 |
6495400 |
missense variant |
A/G;T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs886041009
|
1.000 |
0.120 |
19 |
6495783 |
missense variant |
C/A
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
2 |
2014 |
2014 |
rs886041012
|
1.000 |
0.120 |
19 |
6495599 |
missense variant |
C/A
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs767399782
|
0.925 |
0.120 |
19 |
6495736 |
missense variant |
C/A;T
|
snv
|
4.0E-06
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
2 |
2014 |
2017 |
rs886041010
|
1.000 |
0.120 |
19 |
6495768 |
missense variant |
C/A;T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
2 |
2014 |
2016 |
rs587777429
|
1.000 |
0.120 |
19 |
6496032 |
missense variant |
C/A;T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs886041021
|
1.000 |
0.120 |
19 |
6495327 |
missense variant |
C/A;T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs587777467
|
1.000 |
0.120 |
19 |
6502208 |
missense variant |
C/G;T
|
snv
|
5.7E-06
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
2 |
2014 |
2014 |
rs797045074
|
0.882 |
0.120 |
19 |
6495335 |
missense variant |
C/G;T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
2 |
2014 |
2016 |
rs756762431
|
1.000 |
0.120 |
19 |
6495654 |
missense variant |
C/G;T
|
snv
|
8.0E-06
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs886039470
|
1.000 |
0.120 |
19 |
6495714 |
missense variant |
C/T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
6 |
2014 |
2018 |
rs483352809
|
0.882 |
0.120 |
19 |
6495754 |
missense variant |
C/T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
4 |
2013 |
2014 |
rs587777428
|
0.925 |
0.120 |
19 |
6495271 |
missense variant |
C/T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs886041007
|
1.000 |
0.120 |
19 |
6495769 |
missense variant |
C/T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs886041015
|
1.000 |
0.120 |
19 |
6495445 |
missense variant |
C/T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs886041016
|
1.000 |
0.120 |
19 |
6495438 |
missense variant |
C/T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs761635539
|
1.000 |
0.120 |
19 |
6495931 |
missense variant |
G/A
|
snv
|
4.0E-06
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs886041013
|
1.000 |
0.120 |
19 |
6495558 |
missense variant |
G/A
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs587777468
|
1.000 |
0.120 |
19 |
6495966 |
missense variant |
G/A;C
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
2 |
2014 |
2016 |
rs748787734
|
0.827 |
0.240 |
19 |
6495437 |
missense variant |
G/A;C
|
snv
|
1.2E-05
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2014 |
2014 |
rs587776983
|
0.807 |
0.240 |
19 |
6502209 |
missense variant |
G/A;C;T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
2 |
2013 |
2014 |
rs886041008
|
1.000 |
0.120 |
19 |
6495955 |
missense variant |
G/T
|
snv
|
|
|
Leukodystrophy, Hypomyelinating, 6
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
1.000 |
1 |
2016 |
2016 |