rs10859313
|
|
A |
0.700 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.
|
23853074 |
2014 |
rs4947296
|
|
C |
0.700 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies 6p21 as novel risk locus for dilated cardiomyopathy.
|
23853074 |
2014 |
rs1267969615
|
|
|
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 |
rs397517065
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs397517071
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
|
|
|
rs727504379
|
|
G |
0.700 |
GeneticVariation |
CLINVAR |
Familial left ventricular noncompaction associated with a novel mutation in the alpha-cardiac actin gene.
|
25201647 |
2014 |
rs727502886
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
Mutations in alpha-actinin-2 cause hypertrophic cardiomyopathy: a genome-wide analysis.
|
20022194 |
2010 |
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 |
rs7597774
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genetic association study identifies HSPB7 as a risk gene for idiopathic dilated cardiomyopathy.
|
20975947 |
2010 |
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 |
rs140614802
|
|
A |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs699
|
|
|
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 |
rs867410737
|
|
T |
0.700 |
CausalMutation |
CLINVAR |
Biallelic Mutations in ATP5F1D, which Encodes a Subunit of ATP Synthase, Cause a Metabolic Disorder.
|
29478781 |
2018 |
rs2234962
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
|
21459883 |
2011 |
rs2234962
|
|
|
0.800 |
GeneticVariation |
GWASDB |
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
|
21459883 |
2011 |
rs397516881
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
|
21459883 |
2011 |
rs397516881
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era.
|
22337857 |
2012 |
rs397516881
|
|
A |
0.710 |
CausalMutation |
CLINVAR |
Loss-of-function mutations in co-chaperone BAG3 destabilize small HSPs and cause cardiomyopathy.
|
28737513 |
2017 |
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 |
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 |
rs1554875409
|
|
A |
0.700 |
GeneticVariation |
CLINVAR |
BAG3: a new player in the heart failure paradigm.
|
25925243 |
2015 |
rs1564773559
|
|
CCTGTGTA |
0.700 |
CausalMutation |
CLINVAR |
|
|
|
rs387906875
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
BAG3 myofibrillar myopathy presenting with cardiomyopathy.
|
25728519 |
2015 |
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 |
rs387906875
|
|
T |
0.700 |
GeneticVariation |
CLINVAR |
A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy.
|
21459883 |
2011 |