rs201680145
|
0.882 |
0.200 |
19 |
15179052 |
missense variant |
G/A;T
|
snv
|
8.9E-04
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.720 |
1.000 |
2 |
2012 |
2016 |
rs797045014
|
0.851 |
0.160 |
19 |
15192182 |
missense variant |
G/A;T
|
snv
|
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.710 |
1.000 |
1 |
1997 |
2000 |
rs137852642
|
0.827 |
0.200 |
19 |
15192242 |
missense variant |
G/A;T
|
snv
|
4.5E-06;
4.5E-06
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.100 |
1.000 |
12 |
2000 |
2020 |
rs1555729604
|
0.925 |
0.160 |
19 |
15192449 |
missense variant |
G/A
|
snv
|
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.040 |
1.000 |
4 |
2002 |
2017 |
rs145069047
|
0.925 |
0.160 |
19 |
15192493 |
missense variant |
C/A;G;T
|
snv
|
4.6E-06;
2.6E-04
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.030 |
1.000 |
3 |
2006 |
2020 |
rs201118034
|
0.827 |
0.200 |
19 |
15187315 |
missense variant |
G/A;C
|
snv
|
3.2E-04;
4.0E-06
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.030 |
1.000 |
3 |
2013 |
2015 |
rs28933698
|
0.882 |
0.160 |
19 |
15189004 |
missense variant |
A/G
|
snv
|
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.030 |
1.000 |
3 |
2002 |
2017 |
rs1555727942
|
0.925 |
0.160 |
19 |
15180807 |
missense variant |
G/A
|
snv
|
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.020 |
1.000 |
2 |
2006 |
2009 |
rs75068032
|
0.851 |
0.160 |
19 |
15187273 |
missense variant |
G/A;C;T
|
snv
|
2.4E-05;
5.2E-05
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.020 |
1.000 |
2 |
2013 |
2019 |
rs775836288
|
0.925 |
0.160 |
19 |
15192389 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.020 |
1.000 |
2 |
2006 |
2017 |
rs1188389375
|
1.000 |
0.160 |
19 |
15192193 |
missense variant |
C/A
|
snv
|
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs1328784046
|
0.925 |
0.160 |
19 |
15185502 |
missense variant |
T/C
|
snv
|
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2013 |
2013 |
rs137852641
|
0.925 |
0.160 |
19 |
15191466 |
missense variant |
G/A
|
snv
|
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2005 |
2005 |
rs1438626607
|
1.000 |
0.160 |
19 |
15180173 |
missense variant |
G/A
|
snv
|
|
1.4E-05
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2019 |
2019 |
rs1555730189
|
0.925 |
0.160 |
19 |
15197537 |
missense variant |
G/A
|
snv
|
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2015 |
2015 |
rs28933696
|
0.882 |
0.160 |
19 |
15192134 |
missense variant |
G/A
|
snv
|
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2014 |
2014 |
rs754554486
|
1.000 |
0.160 |
19 |
15187186 |
missense variant |
G/A;C;T
|
snv
|
3.6E-05;
4.0E-06;
4.0E-06
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2017 |
2017 |
rs768965053
|
1.000 |
0.160 |
19 |
15192398 |
missense variant |
G/A;T
|
snv
|
2.4E-05;
4.0E-06
|
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2012 |
2012 |
rs769773673
|
0.925 |
0.160 |
19 |
15187213 |
missense variant |
G/A
|
snv
|
4.0E-05
|
3.5E-05
|
CADASIL Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Nervous System Diseases; Cardiovascular Diseases
|
0.010 |
1.000 |
1 |
2012 |
2012 |