rs199473161
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.
|
15671429 |
2005 |
rs199473161
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Novel SCN5A mutation in amiodarone-responsive multifocal ventricular ectopy-associated cardiomyopathy.
|
24815523 |
2014 |
rs199473161
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Homozygous SCN5A mutation in Brugada syndrome with monomorphic ventricular tachycardia and structural heart abnormalities.
|
17442746 |
2007 |
rs199473161
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
Divergent biophysical defects caused by mutant sodium channels in dilated cardiomyopathy with arrhythmia.
|
18048769 |
2008 |
rs45546039
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
Rare variant mutations in pregnancy-associated or peripartum cardiomyopathy.
|
20458009 |
2010 |
rs45546039
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism.
|
21596231 |
2011 |
rs45546039
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
Spectrum and prevalence of mutations from the first 2,500 consecutive unrelated patients referred for the FAMILION long QT syndrome genetic test.
|
19716085 |
2009 |
rs45546039
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
Coding sequence mutations identified in MYH7, TNNT2, SCN5A, CSRP3, LBD3, and TCAP from 313 patients with familial or idiopathic dilated cardiomyopathy.
|
19412328 |
2008 |
rs45546039
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
Escape capture bigeminy: phenotypic marker of cardiac sodium channel voltage sensor mutation R222Q.
|
22710484 |
2012 |
rs45546039
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
SCN5A rare variants in familial dilated cardiomyopathy decrease peak sodium current depending on the common polymorphism H558R and common splice variant Q1077del.
|
21167004 |
2010 |
rs45546039
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
Criteria to predict carriers of a novel SCN5A mutation in a large Portuguese family affected by the Brugada syndrome.
|
22277643 |
2012 |
rs45546039
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
R222Q SCN5A mutation is associated with reversible ventricular ectopy and dilated cardiomyopathy.
|
22999724 |
2012 |
rs45546039
|
|
T |
0.710 |
CausalMutation |
CLINVAR |
Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy.
|
22766342 |
2012 |
rs727504801
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Sodium channel mutations and susceptibility to heart failure and atrial fibrillation.
|
15671429 |
2005 |
rs727504801
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Genetic basis and molecular mechanism for idiopathic ventricular fibrillation.
|
9521325 |
1998 |
rs727504801
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
Parental electrocardiographic screening identifies a high degree of inheritance for congenital and childhood nonimmune isolated atrioventricular block.
|
22899775 |
2012 |
rs727504801
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
An international compendium of mutations in the SCN5A-encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing.
|
20129283 |
2010 |
rs727504801
|
|
C |
0.700 |
CausalMutation |
CLINVAR |
SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism.
|
21596231 |
2011 |