Gene: BAG3 ×
Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs397516881
rs397516881
BAG3
A 0.710 CausalMutation CLINVAR Loss-of-function mutations in co-chaperone BAG3 destabilize small HSPs and cause cardiomyopathy. 28737513

2017
dbSNP: rs397516881
rs397516881
BAG3
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
BAG3
A 0.710 CausalMutation CLINVAR Evaluating pathogenicity of rare variants from dilated cardiomyopathy in the exome era. 22337857

2012
dbSNP: rs397516881
rs397516881
BAG3
A 0.710 CausalMutation CLINVAR A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. 21459883

2011
dbSNP: rs1554875409
rs1554875409
BAG3
A 0.700 GeneticVariation CLINVAR BAG3: a new player in the heart failure paradigm. 25925243

2015
dbSNP: rs387906875
rs387906875
BAG3
T 0.700 GeneticVariation CLINVAR BAG3 myofibrillar myopathy presenting with cardiomyopathy. 25728519

2015
dbSNP: rs869248137
rs869248137
BAG3
T 0.700 CausalMutation CLINVAR The BAG3 gene variants in Polish patients with dilated cardiomyopathy: four novel mutations and a genotype-phenotype correlation. 25008357

2014
dbSNP: rs869248137
rs869248137
BAG3
T 0.700 CausalMutation CLINVAR Nonsense mutations in BAG3 are associated with early-onset dilated cardiomyopathy in French Canadians. 25448463

2014
dbSNP: rs869248137
rs869248137
BAG3
T 0.700 CausalMutation CLINVAR Titin gene mutations are common in families with both peripartum cardiomyopathy and dilated cardiomyopathy. 24558114

2014
dbSNP: rs387906875
rs387906875
BAG3
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
BAG3
T 0.700 GeneticVariation CLINVAR A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. 21459883

2011
dbSNP: rs727505109
rs727505109
BAG3
G 0.700 GeneticVariation CLINVAR A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. 21459883

2011
dbSNP: rs727505109
rs727505109
BAG3
G 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: rs869248137
rs869248137
BAG3
T 0.700 CausalMutation CLINVAR A genome-wide association study identifies two loci associated with heart failure due to dilated cardiomyopathy. 21459883

2011
dbSNP: rs1564773559
rs1564773559
BAG3
CCTGTGTA 0.700 CausalMutation CLINVAR

dbSNP: rs727502897
rs727502897
BAG3
G 0.700 GeneticVariation CLINVAR

dbSNP: rs727505283
rs727505283
BAG3
A 0.700 GeneticVariation CLINVAR

dbSNP: rs730880055
rs730880055
BAG3
T 0.700 GeneticVariation CLINVAR

dbSNP: rs869025365
rs869025365
BAG3
A 0.700 GeneticVariation CLINVAR

dbSNP: rs876657634
rs876657634
BAG3
T 0.700 GeneticVariation CLINVAR