Gene: MYH7 ×
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 GeneticVariation disease CLINVAR 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 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 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 Multidimensional structure-function relationships in human β-cardiac myosin from population-scale genetic variation. 27247418 2016
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR Identification of novel mutations including a double mutation in patients with inherited cardiomyopathy by a targeted sequencing approach using the Ion Torrent PGM system. 27082122 2016
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Genetic Variants in Isolated Ebstein Anomaly Implicated in Myocardial Development Pathways. 27788187 2016
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Multidimensional structure-function relationships in human β-cardiac myosin from population-scale genetic variation. 27247418 2016
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR The pathogenicity of genetic variants previously associated with left ventricular non-compaction. 27066506 2016
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity. 25611685 2015
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR Results of clinical genetic testing of 2,912 probands with hypertrophic cardiomyopathy: expanded panels offer limited additional sensitivity. 25611685 2015
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain. 25935763 2015
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology. 25741868 2015
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Detection of mutations in symptomatic patients with hypertrophic cardiomyopathy in Taiwan. 25086479 2015
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR Phenotype and prognostic correlations of the converter region mutations affecting the β myosin heavy chain. 25935763 2015
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Novel genotype-phenotype associations demonstrated by high-throughput sequencing in patients with hypertrophic cardiomyopathy. 25351510 2015
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR β-Myosin heavy chain variant Val606Met causes very mild hypertrophic cardiomyopathy in mice, but exacerbates HCM phenotypes in mice carrying other HCM mutations. 24829265 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Distinguishing hypertrophic cardiomyopathy-associated mutations from background genetic noise. 24510615 2014
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 Characterization of a phenotype-based genetic test prediction score for unrelated patients with hypertrophic cardiomyopathy. 24793961 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR Clinical phenotype and outcome of hypertrophic cardiomyopathy associated with thin-filament gene mutations. 25524337 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 CausalMutation disease CLINVAR Genetics of hypertrophic cardiomyopathy in Norway. 24111713 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR DNA sequence capture and next-generation sequencing for the molecular diagnosis of genetic cardiomyopathies. 24183960 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Genetics of hypertrophic cardiomyopathy in Norway. 24111713 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Characterization of a phenotype-based genetic test prediction score for unrelated patients with hypertrophic cardiomyopathy. 24793961 2014
Entrez Id: 4625
Gene Symbol: MYH7
MYH7 		0.700 GeneticVariation disease CLINVAR Mutation analysis of the main hypertrophic cardiomyopathy genes using multiplex amplification and semiconductor next-generation sequencing. 25342278 2014