×
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