Variant Gene Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10927875
rs10927875
0.800 GeneticVariation GWASCAT A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. 21459883

2012

dbSNP: rs10927875
rs10927875
0.800 GeneticVariation GWASDB A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. 21459883

2012

dbSNP: rs2234962
rs2234962
0.800 GeneticVariation GWASCAT A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. 21459883

2012

dbSNP: rs2234962
rs2234962
0.800 GeneticVariation GWASDB A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. 21459883

2012

dbSNP: rs111033560
rs111033560
0.710 CausalMutation CLINVAR Interpreting secondary cardiac disease variants in an exome cohort. 23861362

2014

dbSNP: rs267607554
rs267607554
0.710 GeneticVariation BEFREE The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins. 24001739

2014

dbSNP: rs267607554
rs267607554
0.710 CausalMutation CLINVAR The LMNA mutation p.Arg321Ter associated with dilated cardiomyopathy leads to reduced expression and a skewed ratio of lamin A and lamin C proteins. 24001739

2014

dbSNP: rs267607554
rs267607554
0.710 CausalMutation CLINVAR Risk prediction of ventricular arrhythmias and myocardial function in Lamin A/C mutation positive subjects. 24058181

2014

dbSNP: rs58013325
rs58013325
0.710 GeneticVariation BEFREE This reveals that the LMNA gene insertion mutation (T510Y frameshift mutation) can cause dilated cardiomyopathy, conduction system disease, and sudden cardiac death without skeletal myopathy, clinically manifested with early onset, severe symptoms, and poor prognosis. 23793583

2014

dbSNP: rs267607554
rs267607554
0.710 CausalMutation CLINVAR A systematic approach to assessing the clinical significance of genetic variants. 24033266

2013

dbSNP: rs28933091
rs28933091
0.710 CausalMutation CLINVAR A systematic approach to assessing the clinical significance of genetic variants. 24033266

2013

dbSNP: rs45546039
rs45546039
0.710 CausalMutation CLINVAR Escape capture bigeminy: phenotypic marker of cardiac sodium channel voltage sensor mutation R222Q. 22710484

2013

dbSNP: rs59270054
rs59270054
0.710 CausalMutation CLINVAR A systematic approach to assessing the clinical significance of genetic variants. 24033266

2013

dbSNP: rs59270054
rs59270054
0.710 CausalMutation CLINVAR Identification of a new lamin A/C mutation in a Chinese family affected with atrioventricular block as the prominent phenotype. 20155465

2013

dbSNP: rs74315380
rs74315380
0.710 GeneticVariation CLINVAR A systematic approach to assessing the clinical significance of genetic variants. 24033266

2013

dbSNP: rs45546039
rs45546039
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

dbSNP: rs45546039
rs45546039
0.710 CausalMutation CLINVAR R222Q SCN5A mutation is associated with reversible ventricular ectopy and dilated cardiomyopathy. 22999724

2012

dbSNP: rs45546039
rs45546039
0.710 CausalMutation CLINVAR Multifocal ectopic Purkinje-related premature contractions: a new SCN5A-related cardiac channelopathy. 22766342

2012

dbSNP: rs45546039
rs45546039
0.710 GeneticVariation BEFREE R222Q SCN5A mutation is associated with reversible ventricular ectopy and dilated cardiomyopathy. 22999724

2012

dbSNP: rs74315380
rs74315380
0.710 GeneticVariation CLINVAR Disease-related cardiac troponins alter thin filament Ca2+ association and dissociation rates. 22675533

2012

dbSNP: rs74315380
rs74315380
0.710 GeneticVariation CLINVAR Sarcomere gene mutations in isolated left ventricular noncompaction cardiomyopathy do not predict clinical phenotype. 21551322

2012

dbSNP: rs267607554
rs267607554
0.710 CausalMutation CLINVAR MicroRNA expression profiling in patients with lamin A/C-associated muscular dystrophy. 21840938

2011

dbSNP: rs45546039
rs45546039
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

2011

dbSNP: rs45546039
rs45546039
0.710 CausalMutation CLINVAR SCN5A mutations associate with arrhythmic dilated cardiomyopathy and commonly localize to the voltage-sensing mechanism. 21596231

2011

dbSNP: rs59270054
rs59270054
0.710 CausalMutation CLINVAR LMNA E82K mutation activates FAS and mitochondrial pathways of apoptosis in heart tissue specific transgenic mice. 21151901

2011