< Resources

Download

Mastermind Variant Interpretation Cards

Use Mastermind Variant Interpretation Cards to learn the ACMG Variant Interpretation framework and organize your variant interpretation activities.

Submit the form to download your deck:

Deck Contents
10 Overview Cards

Overview Cards explain the various categories of criteria for interpretation of pathogenic or benign sequence variants (e.g. Pathogenic – Strong Evidence or PS)

5 Scoring Cards

Scoring Cards detail the rules for combining criteria to classify sequence variants (e.g. Likely Pathogenic)

5 Workflow Cards

Workflow Cards describe a proposed process for assessing the pathogenicity of a variant based on the various sources of data (e.g. Literature)

28 Criteria Cards

Criteria Cards detail the features of each criterion for determining pathogenicity or benignness of a variant (e.g. PP3 Predicted Damaging)

The World’s Most Comprehensive Source of Genomic Evidence

Mastermind accelerates variant interpretation with immediate insight into the full text of millions of scientific articles. Prioritize your search results by clinical relevance and find what you are looking for 5-10 times faster

Explore Mastermind CORE
Every Missing Genetic Variant is a Patient Your Label Doesn't Reach
  • Rare disease and precision oncology programs rely on evidence fragmented across millions of published articles and supplemental datasets.
  • Genomenon builds the custom real-world evidence your program needs.
  • AI-powered search. Expert scientific curation.
  • The result: a broader label, more eligible patients, and a regulatory filing your team can defend.
Request a custom evidence build for your program
speak with an expert