Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C3809312
Disease: ATRIAL FIBRILLATION, FAMILIAL, 14
ATRIAL FIBRILLATION, FAMILIAL, 14
0.600 GeneticVariation disease UNIPROT Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477 2009
CUI: C3809312
Disease: ATRIAL FIBRILLATION, FAMILIAL, 14
ATRIAL FIBRILLATION, FAMILIAL, 14
0.600 Biomarker disease CTD_human
CUI: C3809312
Disease: ATRIAL FIBRILLATION, FAMILIAL, 14
ATRIAL FIBRILLATION, FAMILIAL, 14
0.600 CausalMutation disease CLINVAR
CUI: C1142166
Disease: Brugada Syndrome (disorder)
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
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.510 Biomarker disease CLINGEN Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome. 26179811 2015
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.510 Biomarker disease CLINGEN Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort. 26173111 2015
CUI: C1142166
Disease: Brugada Syndrome (disorder)
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
CUI: C1142166
Disease: Brugada Syndrome (disorder)
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
CUI: C1142166
Disease: Brugada Syndrome (disorder)
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
CUI: C1142166
Disease: Brugada Syndrome (disorder)
Brugada Syndrome (disorder)
0.510 Biomarker disease CLINGEN Mutations in sodium channel β1- and β2-subunits associated with atrial fibrillation. 19808477 2009
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias. 27932425 2016
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias
0.300 Biomarker phenotype CLINGEN Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias. 27932425 2016
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder)
0.300 Biomarker disease CLINGEN Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias. 27932425 2016
CUI: C1399226
Disease: Ectopic rhythm
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
CUI: C4551804
Disease: Brugada Syndrome 1
Brugada Syndrome 1
0.300 Biomarker disease CLINGEN Scn2b Deletion in Mice Results in Ventricular and Atrial Arrhythmias. 27932425 2016
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort. 26173111 2015
CUI: C0264893
Disease: Nodal rhythm disorder
Nodal rhythm disorder
0.300 Biomarker phenotype CLINGEN Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome. 26179811 2015
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias
0.300 Biomarker phenotype CLINGEN Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort. 26173111 2015
CUI: C0348626
Disease: Other specified cardiac arrhythmias
Other specified cardiac arrhythmias
0.300 Biomarker phenotype CLINGEN Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome. 26179811 2015
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder)
0.300 Biomarker disease CLINGEN Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort. 26173111 2015
CUI: C0428908
Disease: Sinus Node Dysfunction (disorder)
Sinus Node Dysfunction (disorder)
0.300 Biomarker disease CLINGEN Contribution of Cardiac Sodium Channel β-Subunit Variants to Brugada Syndrome. 26179811 2015
CUI: C1399226
Disease: Ectopic rhythm
Ectopic rhythm
0.300 Biomarker phenotype CLINGEN Comprehensive Genetic Characterization of a Spanish Brugada Syndrome Cohort. 26173111 2015
CUI: C1399226
Disease: Ectopic rhythm
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