rs74315447
|
0.925 |
0.120 |
21 |
34370639 |
missense variant |
T/C
|
snv
|
2.6E-04
|
2.3E-04
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.800 |
1.000 |
4 |
1999 |
2009 |
rs74315448
|
1.000 |
0.120 |
21 |
34370648 |
missense variant |
T/C
|
snv
|
1.1E-03
|
6.1E-04
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.800 |
1.000 |
4 |
1999 |
2009 |
rs141423405
|
1.000 |
0.120 |
21 |
34370707 |
missense variant |
C/T
|
snv
|
6.4E-05
|
4.2E-05
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
4 |
1999 |
2009 |
rs199473363
|
1.000 |
0.120 |
21 |
34370537 |
missense variant |
T/A
|
snv
|
|
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
4 |
1999 |
2009 |
rs199473364
|
1.000 |
0.120 |
21 |
34370671 |
missense variant |
G/A;C
|
snv
|
2.0E-05;
2.4E-05
|
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
4 |
1999 |
2009 |
rs199473365
|
1.000 |
0.120 |
21 |
34370708 |
missense variant |
G/A
|
snv
|
8.0E-06
|
7.0E-06
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
4 |
1999 |
2009 |
rs74424227
|
1.000 |
0.120 |
21 |
34370759 |
missense variant |
A/G
|
snv
|
1.0E-04
|
2.1E-05
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
4 |
1999 |
2009 |
rs74315449
|
0.882 |
0.120 |
21 |
34370557 |
missense variant |
C/A;T
|
snv
|
4.0E-06;
1.3E-04
|
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
1 |
2004 |
2004 |
rs142153692
|
1.000 |
0.120 |
21 |
34370518 |
missense variant |
G/A;C
|
snv
|
1.9E-04;
4.0E-06
|
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs148968498
|
1.000 |
0.120 |
21 |
34370558 |
missense variant |
G/A
|
snv
|
6.4E-05
|
2.4E-04
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|
rs16991654
|
0.925 |
0.120 |
21 |
34370656 |
missense variant |
T/A;C
|
snv
|
4.0E-06
|
|
Long Qt Syndrome 6
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
|
0 |
|
|