Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 Biomarker disease GENOMICS_ENGLAND Reassessment of Mendelian gene pathogenicity using 7,855 cardiomyopathy cases and 60,706 reference samples. 27532257 2017
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR Malignant effects of multiple rare variants in sarcomere genes on the prognosis of patients with hypertrophic cardiomyopathy. 25132132 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR New population-based exome data are questioning the pathogenicity of previously cardiomyopathy-associated genetic variants. 23299917 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR Abnormal calcium handling properties underlie familial hypertrophic cardiomyopathy pathology in patient-specific induced pluripotent stem cells. 23290139 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR Multiple gene mutations, not the type of mutation, are the modifier of left ventricle hypertrophy in patients with hypertrophic cardiomyopathy. 23283745 2013
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease UNIPROT Clinical and mutational spectrum in a cohort of 105 unrelated patients with dilated cardiomyopathy. 21846512 2012
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease UNIPROT Mutations in the sarcomere gene MYH7 in Ebstein anomaly. 21127202 2011
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR Haplotype sharing test maps genes for familial cardiomyopathies. 20573160 2011
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 Biomarker disease GENOMICS_ENGLAND The genetics of dilated cardiomyopathy. 20186049 2010
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease UNIPROT Mutations in sarcomere protein genes in left ventricular noncompaction. 18506004 2008
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease UNIPROT Mutation screening in dilated cardiomyopathy: prominent role of the beta myosin heavy chain gene. 15769782 2005
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease UNIPROT Novel mutations in sarcomeric protein genes in dilated cardiomyopathy. 12379228 2002
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease UNIPROT Mutations in sarcomere protein genes as a cause of dilated cardiomyopathy. 11106718 2000
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR Familial hypertrophic cardiomyopathy and atrial fibrillation caused by Arg663His beta-cardiac myosin heavy chain mutation. 10750581 1999
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 Biomarker disease CTD_human
Entrez Id: 4000
Gene Symbol: LMNA
LMNA 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 1674
Gene Symbol: DES
DES 		0.100 CausalMutation disease CLINVAR
Entrez Id: 282996
Gene Symbol: RBM20
RBM20 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 4633
Gene Symbol: MYL2
MYL2 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 282996
Gene Symbol: RBM20
RBM20 		0.100 CausalMutation disease CLINVAR
Entrez Id: 4000
Gene Symbol: LMNA
LMNA 		0.100 CausalMutation disease CLINVAR
Entrez Id: 7273
Gene Symbol: TTN
TTN 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 5318
Gene Symbol: PKP2
PKP2 		0.100 GeneticVariation disease CLINVAR
Entrez Id: 91624
Gene Symbol: NEXN
NEXN 		0.100 GeneticVariation disease CLINVAR