rs398123234
|
1.000 |
0.120 |
7 |
65974686 |
missense variant |
C/T
|
snv
|
8.0E-06
|
7.0E-06
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs121918185
|
0.925 |
0.280 |
7 |
65974701 |
stop gained |
G/A
|
snv
|
2.4E-05
|
2.1E-05
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
6 |
1993 |
2015 |
rs121918185
|
0.925 |
0.280 |
7 |
65974701 |
stop gained |
G/A
|
snv
|
2.4E-05
|
2.1E-05
|
Hydrops Fetalis, Non-Immune
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs121918175
|
1.000 |
0.120 |
7 |
65974923 |
missense variant |
G/A
|
snv
|
8.0E-06
|
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
13 |
1991 |
2003 |
rs191153460
|
1.000 |
0.120 |
7 |
65974933 |
missense variant |
G/A
|
snv
|
2.0E-05
|
7.0E-06
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs121918182
|
1.000 |
0.120 |
7 |
65974934 |
missense variant |
C/G;T
|
snv
|
3.2E-05
|
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
13 |
1991 |
2003 |
rs531607427
|
1.000 |
0.120 |
7 |
65974942 |
missense variant |
C/T
|
snv
|
|
7.0E-06
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.010 |
1.000 |
1 |
2005 |
2005 |
rs886044680
|
1.000 |
0.120 |
7 |
65975025 |
missense variant |
T/G
|
snv
|
8.0E-06
|
7.0E-06
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1451709678
|
1.000 |
0.120 |
7 |
65976034 |
missense variant |
G/A
|
snv
|
|
7.0E-06
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs121918174
|
1.000 |
0.120 |
7 |
65979477 |
missense variant |
G/A
|
snv
|
2.0E-05
|
7.0E-06
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
13 |
1991 |
2003 |
rs587779400
|
1.000 |
0.120 |
7 |
65979778 |
missense variant |
G/A
|
snv
|
|
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs121918181
|
0.882 |
0.120 |
7 |
65979782 |
missense variant |
G/A
|
snv
|
5.6E-05
|
7.0E-05
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.820 |
1.000 |
14 |
1991 |
2003 |
rs121918181
|
0.882 |
0.120 |
7 |
65979782 |
missense variant |
G/A
|
snv
|
5.6E-05
|
7.0E-05
|
Mucopolysaccharidosis VI
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
7 |
1994 |
2018 |
rs121918181
|
0.882 |
0.120 |
7 |
65979782 |
missense variant |
G/A
|
snv
|
5.6E-05
|
7.0E-05
|
Mucopolysaccharidoses
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.010 |
1.000 |
1 |
1994 |
1994 |
rs121918177
|
1.000 |
0.120 |
7 |
65979866 |
missense variant |
G/A
|
snv
|
|
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.800 |
1.000 |
13 |
1991 |
2003 |
rs1417426295
|
1.000 |
0.120 |
7 |
65979902 |
missense variant |
C/T
|
snv
|
|
7.0E-06
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
13 |
1991 |
2003 |
rs786205671
|
1.000 |
0.200 |
7 |
65979910 |
missense variant |
C/G
|
snv
|
|
|
Hydrops Fetalis, Non-Immune
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs786205673
|
1.000 |
0.200 |
7 |
65980313 |
missense variant |
G/A
|
snv
|
1.6E-05
|
7.0E-06
|
Hydrops Fetalis, Non-Immune
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Female Urogenital Diseases and Pregnancy Complications; Immune System Diseases; Hemic and Lymphatic Diseases
|
0.700 |
1.000 |
1 |
2015 |
2015 |
rs1424546265
|
1.000 |
0.120 |
7 |
65982029 |
missense variant |
G/A
|
snv
|
8.3E-06
|
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
1.000 |
13 |
1991 |
2003 |
rs779499448
|
1.000 |
0.120 |
7 |
65982072 |
missense variant |
A/C;G
|
snv
|
4.2E-06;
4.2E-06
|
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs1238361161
|
1.000 |
0.120 |
7 |
65982080 |
stop gained |
G/T
|
snv
|
|
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|
rs747792546
|
1.000 |
0.120 |
7 |
65982096 |
missense variant |
G/A;T
|
snv
|
4.5E-06;
4.5E-06
|
|
Mucopolysaccharidosis VII
|
Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nutritional and Metabolic Diseases; Skin and Connective Tissue Diseases
|
0.700 |
|
0 |
|
|