Interpreting Incidentally Identified Variants in Genes Associated with Heritable Cardiovascular Disease: A Scientific Statement from the American Heart Association

Keyphrases

• Cardiovascular Disease 100%
• Scientific Statement 100%
• Clinical Evaluation 66%
• Genetic Variants 66%
• Dyslipidemia 33%
• Monogenic 33%
• Exome Sequencing 33%
• Clinical Management 33%
• Cardiomyopathy 33%
• Clinical Application 33%
• Pathogenicity 33%
• Genome Sequencing 33%
• Consensus Statement 33%
• Associated Diseases 33%
• Disease Genes 33%
• Multidisciplinary Team 33%
• Genomic Medicine 33%
• Clinical Care 33%
• Incidental 33%
• Genomic Technologies 33%
• Structural Heart Disease 33%
• Patient's Family 33%
• Thoracic Aortic Disease 33%
• Diagnostic Research 33%
• Cardiac Channelopathies 33%
• Direct-to-consumer 33%
• Cardiovascular Genomics 33%

Medicine and Dentistry

• Clinician 100%
• Cardiovascular Disease 100%
• Clinical Trial 66%
• Disease 66%
• Cardiovascular System 33%
• Diagnosis 33%
• Medicine 33%
• Heart Disease 33%
• Genetic Variability 33%
• Dyslipidemia 33%
• Clinical Management 33%
• Genome Sequencing 33%
• Aortic Disease 33%
• Exome Sequencing 33%
• Myocardial Disease 33%
• Channelopathy 33%
• Consumer 33%
• Pathogenicity 33%

Biochemistry, Genetics and Molecular Biology

• Clinical Trial 100%
• Genetic Divergence 100%
• Dyslipidemia 50%
• Genetics 50%
• Genome Sequencing 50%
• Exome Sequencing 50%
• Channelopathy 50%
• Genomics 50%