|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.600 |
Biomarker
|
disease |
CLINGEN |
Cardiac conduction defects and Brugada syndrome: A family with overlap syndrome carrying a nonsense SCN5A mutation.
|
28217227 |
2017 |
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.600 |
Biomarker
|
disease |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.600 |
Biomarker
|
disease |
CLINGEN |
Scn1b deletion leads to increased tetrodotoxin-sensitive sodium current, altered intracellular calcium homeostasis and arrhythmias in murine hearts.
|
25772295 |
2015 |
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.600 |
Biomarker
|
disease |
CLINGEN |
SCN1B gene variants in Brugada Syndrome: a study of 145 SCN5A-negative patients.
|
25253298 |
2014 |
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.600 |
Biomarker
|
disease |
CLINGEN |
SCN1Bb R214Q found in 3 patients: 1 with Brugada syndrome and 2 with lone atrial fibrillation.
|
22155598 |
2012 |
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.600 |
Biomarker
|
disease |
CLINGEN |
A novel rare variant in SCN1Bb linked to Brugada syndrome and SIDS by combined modulation of Na(v)1.5 and K(v)4.3 channel currents.
|
22155597 |
2012 |
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.600 |
Biomarker
|
disease |
CLINGEN |
Sodium channel β1 subunit mutations associated with Brugada syndrome and cardiac conduction disease in humans.
|
18464934 |
2008 |
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.600 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
|
| Entrez Id: |
6324 |
| Gene Symbol: |
SCN1B |
SCN1B
|
0.600 |
CausalMutation
|
disease |
CLINVAR |
|
|
|
|
| Entrez Id: |
6336 |
| Gene Symbol: |
SCN10A |
SCN10A
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Association of common and rare variants of SCN10A gene with sudden unexplained nocturnal death syndrome in Chinese Han population.
|
27272739 |
2017 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Embryonic type Na+ channel β-subunit, SCN3B masks the disease phenotype of Brugada syndrome.
|
27677334 |
2016 |
|
| Entrez Id: |
6327 |
| Gene Symbol: |
SCN2B |
SCN2B
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias.
|
27932425 |
2016 |
|
| Entrez Id: |
6336 |
| Gene Symbol: |
SCN10A |
SCN10A
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Novel SCN10A variants associated with Brugada syndrome.
|
25842276 |
2016 |
|
| Entrez Id: |
10021 |
| Gene Symbol: |
HCN4 |
HCN4
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Mutation in S6 domain of HCN4 channel in patient with suspected Brugada syndrome modifies channel function.
|
27553229 |
2016 |
|
| Entrez Id: |
6336 |
| Gene Symbol: |
SCN10A |
SCN10A
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Contrasting Nav1.8 Activity in Scn10a-/- Ventricular Myocytes and the Intact Heart.
|
27806966 |
2016 |
|
| Entrez Id: |
5318 |
| Gene Symbol: |
PKP2 |
PKP2
|
0.300 |
Biomarker
|
disease |
CLINGEN |
High prevalence of concealed Brugada syndrome in patients with atrioventricular nodal reentrant tachycardia.
|
25998140 |
2015 |
|
CACNA2D1
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Functional characterization of CaVα2δ mutations associated with sudden cardiac death.
|
25527503 |
2015 |
|
| Entrez Id: |
55800 |
| Gene Symbol: |
SCN3B |
SCN3B
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
|
| Entrez Id: |
5318 |
| Gene Symbol: |
PKP2 |
PKP2
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Epicardial Ventricular Tachycardia Ablation in a Patient With Brugada ECG Pattern and Mutation of PKP2 and DSP Genes.
|
25900994 |
2015 |
|
| Entrez Id: |
3752 |
| Gene Symbol: |
KCND3 |
KCND3
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Two novel Brugada syndrome-associated mutations increase KV4.3 membrane expression and function.
|
26016905 |
2015 |
|
| Entrez Id: |
6327 |
| Gene Symbol: |
SCN2B |
SCN2B
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort.
|
26173111 |
2015 |
|
| Entrez Id: |
6327 |
| Gene Symbol: |
SCN2B |
SCN2B
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome.
|
26179811 |
2015 |
|
| Entrez Id: |
6336 |
| Gene Symbol: |
SCN10A |
SCN10A
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study.
|
25691538 |
2015 |
|
| Entrez Id: |
5318 |
| Gene Symbol: |
PKP2 |
PKP2
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Missense mutations in plakophilin-2 cause sodium current deficit and associate with a Brugada syndrome phenotype.
|
24352520 |
2014 |
|
| Entrez Id: |
3764 |
| Gene Symbol: |
KCNJ8 |
KCNJ8
|
0.300 |
Biomarker
|
disease |
CLINGEN |
Role of ATP-sensitive K+ channels in cardiac arrhythmias.
|
24367007 |
2014 |