Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10859313
rs10859313
A 0.700 GeneticVariation GWASDB A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy. 23853074

2014

dbSNP: rs4947296
rs4947296
C 0.700 GeneticVariation GWASDB A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy. 23853074

2014

dbSNP: rs1267969615
rs1267969615
ACE
0.010 GeneticVariation BEFREE We examined frequencies of the M235T variant of angiotensinogen gene and I/D polymorphism of gene for angiotensin-converting enzyme in Slovak population: in hypertensive patients, coronary heart disease (CHD), dilated cardiomyopathy (DCM) and myocardial infarction (MI) patients compared to healthy subjects. 17579251

2007

dbSNP: rs397517065
rs397517065
A 0.700 GeneticVariation CLINVAR

dbSNP: rs397517071
rs397517071
G 0.700 GeneticVariation CLINVAR

dbSNP: rs727504379
rs727504379
G 0.700 GeneticVariation CLINVAR Familial left ventricular noncompaction associated with a novel mutation in the alpha-cardiac actin gene. 25201647

2014

dbSNP: rs727502886
rs727502886
A 0.700 CausalMutation CLINVAR Mutations in alpha-actinin-2 cause hypertrophic cardiomyopathy: a genome-wide analysis. 20022194

2010

dbSNP: rs1407369744
rs1407369744
0.010 GeneticVariation BEFREE Whole-Exome Sequencing Identifies a Novel Mutation (p.L320R) of Alpha-Actinin 2 in a Chinese Family with Dilated Cardiomyopathy and Ventricular Tachycardia. 30630173

2019

dbSNP: rs7597774
rs7597774
0.700 GeneticVariation GWASDB Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy. 20975947

2010

dbSNP: rs1801253
rs1801253
0.010 GeneticVariation BEFREE In vitro, the Gly389 variant of beta1-AR mediates less adenylyl cyclase activities than the Arg389 variant, so Arg389Gly polymorphism was investigated with regard to the genesis, progression, or arrhythmogenesis of dilated cardiomyopathy (DCM). 12197595

2002

dbSNP: rs140614802
rs140614802
A 0.700 CausalMutation CLINVAR

dbSNP: rs699
rs699
AGT
0.010 GeneticVariation BEFREE We examined frequencies of the M235T variant of angiotensinogen gene and I/D polymorphism of gene for angiotensin-converting enzyme in Slovak population: in hypertensive patients, coronary heart disease (CHD), dilated cardiomyopathy (DCM) and myocardial infarction (MI) patients compared to healthy subjects. 17579251

2007

dbSNP: rs867410737
rs867410737
T 0.700 CausalMutation CLINVAR Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder. 29478781

2018

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

2011

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

2011

dbSNP: rs397516881
rs397516881
A 0.710 CausalMutation CLINVAR A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. 21459883

2011

dbSNP: rs397516881
rs397516881
A 0.710 CausalMutation CLINVAR Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era. 22337857

2012

dbSNP: rs397516881
rs397516881
A 0.710 CausalMutation CLINVAR Loss-of-function mutations in co-chaperone BAG3 destabilize small HSPs and cause cardiomyopathy. 28737513

2017

dbSNP: rs397516881
rs397516881
A 0.710 CausalMutation CLINVAR The BAG3 gene variants in Polish patients with dilated cardiomyopathy: four novel mutations and a genotype-phenotype correlation. 25008357

2014

dbSNP: rs397516881
rs397516881
0.710 GeneticVariation BEFREE Mutation and downregulation of the co-chaperone protein BCL-2-associated athanogene 3 (BAG3) are associated with cardiac myopathy and heart failure, and a BAG3 E455K mutation leads to dilated cardiomyopathy (DCM). 28737513

2017

dbSNP: rs1554875409
rs1554875409
A 0.700 GeneticVariation CLINVAR BAG3: a new player in the heart failure paradigm. 25925243

2015

dbSNP: rs1564773559
rs1564773559
CCTGTGTA 0.700 CausalMutation CLINVAR

dbSNP: rs387906875
rs387906875
T 0.700 GeneticVariation CLINVAR BAG3 myofibrillar myopathy presenting with cardiomyopathy. 25728519

2015

dbSNP: rs387906875
rs387906875
T 0.700 GeneticVariation CLINVAR Genome-wide studies of copy number variation and exome sequencing identify rare variants in BAG3 as a cause of dilated cardiomyopathy. 21353195

2011

dbSNP: rs387906875
rs387906875
T 0.700 GeneticVariation CLINVAR A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. 21459883

2011