Consensus recommendations on the interpretation of sequence variants from the American College of Medical Genetics and Genomics (ACMG) and the Association for Molecular Pathology (AMP).
Consensus recommendations on the interpretation and reporting of constitutional copy-number variants from the American College of Medical Genetics and Genomics (ACMG) and the Clinical Genome Resource (ClinGen).
ClinGen guidelines for applying ACMG/AMP variant interpretation criteria, with criteria-specific recommendations.
Professional network providing consensus specifications, recommendations, and supporting resources for cancer variant interpretation.
ACGS guidelines for clinical genomics, including standards and recommendations relevant to genetic testing and variant interpretation workflows.
AMP guidelines and recommendations for genetic and genomic testing methodologies, variant interpretation, and reporting.
