rs199472805
|
0.925 |
0.120 |
11 |
2777000 |
missense variant |
T/C;G
|
snv
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
9 |
2005 |
2015 |
rs397508097
|
0.807 |
0.120 |
11 |
2768917 |
stop gained |
C/T
|
snv
|
2.8E-05
|
1.4E-05
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
9 |
2001 |
2014 |
rs120074178
|
0.925 |
0.120 |
11 |
2570719 |
missense variant |
G/A;C;T
|
snv
|
4.0E-06;
4.0E-06;
1.6E-05
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
8 |
1996 |
2014 |
rs199472696
|
0.851 |
0.120 |
11 |
2570670 |
missense variant |
C/T
|
snv
|
4.0E-06
|
1.4E-05
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
8 |
1997 |
2013 |
rs199472800
|
0.925 |
0.120 |
11 |
2776033 |
missense variant |
G/A;T
|
snv
|
2.3E-05;
5.7E-06
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
8 |
1997 |
2014 |
rs179489
|
0.925 |
0.120 |
11 |
2570652 |
missense variant |
G/A;C
|
snv
|
1.2E-05;
4.0E-06
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
7 |
1998 |
2015 |
rs199472687
|
0.827 |
0.120 |
11 |
2527962 |
missense variant |
G/A
|
snv
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
7 |
2005 |
2015 |
rs199472709
|
0.790 |
0.120 |
11 |
2572021 |
missense variant |
G/A;T
|
snv
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
7 |
2004 |
2015 |
rs199472713
|
0.925 |
0.120 |
11 |
2572056 |
missense variant |
C/A;T
|
snv
|
4.0E-06
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
7 |
1999 |
2015 |
rs120074194
|
0.925 |
0.120 |
11 |
2572871 |
missense variant |
G/A;T
|
snv
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
6 |
1997 |
2007 |
rs199472720
|
0.925 |
0.120 |
11 |
2572105 |
missense variant |
G/A;T
|
snv
|
1.6E-05
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
6 |
2000 |
2015 |
rs199472790
|
0.925 |
0.120 |
11 |
2768900 |
missense variant |
T/G
|
snv
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
6 |
2003 |
2013 |
rs397508104
|
0.925 |
0.120 |
11 |
2847859 |
frameshift variant |
C/-;CC
|
delins
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
6 |
1999 |
2014 |
rs775537394
|
1.000 |
0.120 |
11 |
2661960 |
splice acceptor variant |
G/T
|
snv
|
4.0E-06
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
6 |
1997 |
2016 |
rs794728537
|
0.925 |
0.120 |
11 |
2778023 |
stop gained |
C/T
|
snv
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
6 |
1999 |
2014 |
rs120074177
|
0.925 |
0.120 |
11 |
2570682 |
missense variant |
G/A;C
|
snv
|
4.0E-06
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
5 |
1997 |
2014 |
rs1554895166
|
1.000 |
0.120 |
11 |
2588718 |
frameshift variant |
G/-
|
del
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
5 |
2004 |
2012 |
rs1800171
|
0.882 |
0.120 |
11 |
2583545 |
splice region variant |
G/A;C;T
|
snv
|
4.0E-06
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
5 |
1998 |
2012 |
rs199472706
|
0.925 |
0.120 |
11 |
2571391 |
missense variant |
C/T
|
snv
|
4.0E-06
|
1.0E-04
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
5 |
2005 |
2016 |
rs199472755
|
0.851 |
0.120 |
11 |
2583478 |
missense variant |
C/A;G;T
|
snv
|
4.0E-06
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
5 |
2005 |
2012 |
rs397508083
|
1.000 |
0.120 |
11 |
2588719 |
frameshift variant |
A/-;AA
|
delins
|
|
7.0E-06
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
5 |
2004 |
2012 |
rs397508118
|
0.851 |
0.120 |
11 |
2570720 |
frameshift variant |
GCGCT/-
|
delins
|
|
1.4E-05
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
5 |
1999 |
2015 |
rs139042529
|
0.925 |
0.120 |
11 |
2570663 |
stop gained |
C/A;G;T
|
snv
|
8.0E-06;
9.4E-04
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
4 |
2005 |
2015 |
rs397508068
|
1.000 |
0.120 |
11 |
2583527 |
inframe deletion |
CTT/-
|
delins
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
4 |
1998 |
2016 |
rs1564886323
|
1.000 |
0.120 |
11 |
2768842 |
splice acceptor variant |
AG/-
|
del
|
|
|
Long QT Syndrome
|
Pathological Conditions, Signs and Symptoms; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Cardiovascular Diseases
|
0.700 |
1.000 |
3 |
1997 |
2009 |