ATRIAL FIBRILLATION, FAMILIAL, 14
|
0.600 |
GeneticVariation
|
disease |
UNIPROT |
Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation.
|
19808477 |
2009 |
ATRIAL FIBRILLATION, FAMILIAL, 14
|
0.600 |
Biomarker
|
disease |
CTD_human |
|
|
|
ATRIAL FIBRILLATION, FAMILIAL, 14
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
Brugada Syndrome (disorder)
|
0.510 |
Biomarker
|
disease |
CLINGEN |
Mutations in SCN2B, encoding voltage-gated sodium channel β2-subunits, are associated with human cardiac arrhythmias, including atrial fibrillation and Brugada syndrome.
|
27932425 |
2016 |
Brugada Syndrome (disorder)
|
0.510 |
Biomarker
|
disease |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
Brugada Syndrome (disorder)
|
0.510 |
Biomarker
|
disease |
CLINGEN |
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
|
26173111 |
2015 |
Brugada Syndrome (disorder)
|
0.510 |
Biomarker
|
disease |
CLINGEN |
The effect of the mutant β2 subunit on the INa strongly suggests that SCN2B is a new candidate gene associated with BrS.
|
23559163 |
2013 |
Brugada Syndrome (disorder)
|
0.510 |
GeneticVariation
|
disease |
ORPHANET |
The effect of the mutant β2 subunit on the INa strongly suggests that SCN2B is a new candidate gene associated with BrS.
|
23559163 |
2013 |
Brugada Syndrome (disorder)
|
0.510 |
Biomarker
|
disease |
BEFREE |
The effect of the mutant β2 subunit on the INa strongly suggests that SCN2B is a new candidate gene associated with BrS.
|
23559163 |
2013 |
Brugada Syndrome (disorder)
|
0.510 |
Biomarker
|
disease |
CLINGEN |
Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation.
|
19808477 |
2009 |
Nodal rhythm disorder
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
|
27932425 |
2016 |
Other specified cardiac arrhythmias
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
|
27932425 |
2016 |
Sinus Node Dysfunction (disorder)
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
|
27932425 |
2016 |
Ectopic rhythm
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
|
27932425 |
2016 |
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
|
27932425 |
2016 |
Brugada Syndrome 1
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
|
27932425 |
2016 |
Nodal rhythm disorder
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
|
26173111 |
2015 |
Nodal rhythm disorder
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
Other specified cardiac arrhythmias
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
|
26173111 |
2015 |
Other specified cardiac arrhythmias
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
Sinus Node Dysfunction (disorder)
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
|
26173111 |
2015 |
Sinus Node Dysfunction (disorder)
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
Ectopic rhythm
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
|
26173111 |
2015 |
Ectopic rhythm
|
0.300 |
Biomarker
|
phenotype |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
CARDIAC CONDUCTION DEFECT, NONSPECIFIC (disorder)
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
|
26173111 |
2015 |