rs148092995
|
1.000 |
0.120 |
22 |
50626154 |
missense variant |
C/T
|
snv
|
1.3E-05
|
2.1E-05
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
0 |
2003 |
2017 |
rs199476359
|
1.000 |
0.120 |
22 |
50626216 |
missense variant |
G/A
|
snv
|
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
|
0 |
|
|
rs199476366
|
1.000 |
0.120 |
22 |
50626708 |
missense variant |
C/T
|
snv
|
1.2E-05
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
0 |
1997 |
2016 |
rs199476382
|
1.000 |
0.120 |
22 |
50626195 |
missense variant |
C/T
|
snv
|
8.3E-06
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
0 |
1995 |
2017 |
rs74315459
|
0.925 |
0.120 |
22 |
50626202 |
missense variant |
C/A;T
|
snv
|
2.9E-05
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
0 |
1993 |
2016 |
rs74315471
|
0.925 |
0.120 |
22 |
50626706 |
missense variant |
C/T
|
snv
|
1.2E-05
|
7.0E-06
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
0 |
1993 |
2017 |
rs74315480
|
1.000 |
0.120 |
22 |
50625615 |
missense variant |
G/A;C
|
snv
|
1.6E-05;
4.0E-06
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
0 |
1995 |
2011 |
rs74315483
|
0.925 |
0.120 |
22 |
50626682 |
missense variant |
C/T
|
snv
|
4.0E-06
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.800 |
1.000 |
0 |
2002 |
2008 |
rs199476357
|
1.000 |
0.120 |
22 |
50627619 |
missense variant |
A/G
|
snv
|
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.710 |
1.000 |
0 |
2006 |
2006 |
rs199476361
|
1.000 |
0.120 |
22 |
50625453 |
missense variant |
T/C
|
snv
|
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.710 |
1.000 |
0 |
2006 |
2006 |
rs199476374
|
1.000 |
0.120 |
22 |
50626941 |
missense variant |
G/T
|
snv
|
8.0E-06
|
7.0E-06
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.710 |
1.000 |
0 |
1999 |
1999 |
rs199476383
|
1.000 |
0.120 |
22 |
50626857 |
missense variant |
A/C
|
snv
|
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.710 |
1.000 |
0 |
2005 |
2005 |
rs199476385
|
1.000 |
0.120 |
22 |
50625263 |
missense variant |
G/C
|
snv
|
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.710 |
1.000 |
0 |
2003 |
2003 |
rs199476390
|
1.000 |
0.120 |
22 |
50626191 |
missense variant |
C/A;T
|
snv
|
2.1E-05;
4.1E-06
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.710 |
1.000 |
0 |
2000 |
2000 |
rs28940895
|
0.925 |
0.120 |
22 |
50625446 |
missense variant |
G/A
|
snv
|
4.2E-06
|
7.0E-06
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.710 |
1.000 |
0 |
2001 |
2001 |
rs60504011
|
1.000 |
0.120 |
22 |
50627219 |
missense variant |
G/A;C;T
|
snv
|
8.4E-06;
4.2E-06
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.710 |
1.000 |
0 |
2003 |
2003 |
rs6151425
|
0.925 |
0.160 |
22 |
50625640 |
missense variant |
G/A;C;T
|
snv
|
3.4E-02
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.710 |
1.000 |
0 |
2003 |
2003 |
rs121434215
|
0.925 |
0.120 |
22 |
50627221 |
missense variant |
A/G
|
snv
|
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs148403406
|
1.000 |
0.120 |
22 |
50626862 |
missense variant |
C/T
|
snv
|
5.6E-05
|
2.1E-04
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs199476339
|
1.000 |
0.120 |
22 |
50627721 |
missense variant |
G/A;T
|
snv
|
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs199476340
|
1.000 |
0.120 |
22 |
50627686 |
missense variant |
C/G
|
snv
|
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs199476341
|
1.000 |
0.120 |
22 |
50626878 |
missense variant |
C/G;T
|
snv
|
8.0E-06
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs199476342
|
1.000 |
0.120 |
22 |
50626594 |
missense variant |
T/C
|
snv
|
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs199476343
|
1.000 |
0.120 |
22 |
50626221 |
missense variant |
C/G
|
snv
|
|
7.0E-06
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|
rs199476344
|
1.000 |
0.120 |
22 |
50625657 |
missense variant |
A/T
|
snv
|
|
|
Leukodystrophy, Metachromatic
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Nervous System Diseases
|
0.700 |
|
0 |
|
|