Genomenon Resources

Offerings

Uses

The Race

Create a mastermind account

A computer in a clinical lab using Mastermind genomic database software.

Software Solutions

Explore our platforms for germline and somatic variant interpretation 

Access article information on more than 26 million variants, as well as curated germline variant content.

Meet Mastermind

Our Cancer Knowledgebase is used to interpret cancer variants, connecting them to therapies and clinical trials 

Meet CKB

Services

Partner with our team of experts to create Tailored Solutions for your unique needs

Clinical Diagnostic Services

Precision Therapeutics Services

Data

Gain access to an expansive, constantly updated database of curated genomic information

Learn More

Clinical Diagnostics

Precision Therapeutics

Software Solutions

Services

Data

Resources

Find your resource

Future Proof Your Lab: Streamline Variant Interpretation with Automation

Welcome to Mastermind CORE powered by Genomenon

Systematic Literature Review of GLA Variants Uncovers Additional Fabry Disease-Causing Variants

Hartwig Medical Foundation Accelerating Cancer Diagnostics CKB Case Study

ACMG Annual Clinical Genetics Meeting 2025 Exhibit Theater Presentation

Genomenon Making Genomic Evidence Actionable

Leveraging Genomic Data to Transform Rare Cancer Treatment

Functional Effects of Variants Quick Reference

AMP 2024 Corporate Workshop

Novel Gene-Disease Relationship Classification Framework, Comparison ClinGen Standard

Biochemical Data in Published Patient Reports Familial Hypercholesterolemia

Comprehensive Identification of Gene-Disease Relationships Across the Clinical Exome

Estimation Global Genetic Prevalence PLA2G6-Associated Neurodegeneration

Reclassification Genetic Variants Unknown Pathogenicity Inherited Myeloidneoplasms

RET Oncogene Medullary Thyroid Carcinoma Patient Management

ASHG CoLab Presentation

Curated Evidence and Article Viewer

Future Proof Your Lab: Streamline Variant Interpretation with Evidence Automation

CKB Cancer Knowledgebase Tutorial

Featured Gene: C3

Mastermind in Action Improving LGMD Patient Outcomes

Featured Gene: NPC1

Using Somatic Variant Curation to Interpret Complex Cancer Genomic Profiles

How Pharming is Partnering Genomenon Democratize Access Genetic Evidence Promote Earlier APDS Diagnosis

How Loxo@Lilly Partnered with Genomenon Refine CDx Submission Retevmo®

How Inozyme is Partnering Genomenon Raise Awareness Promote Earlier Diagnosis ENPP1 Deficiency

Advancing Fabry Disease Diagnosis

Hot Topics Report Clinical Diagnostics 2024

Correcting the Record, Data Integrity in Comparison Studies

Mastermind User Group Meeting 2024

Prognosis Potential: POLE PIK3R1 Changing Approach Endometrial Cancer

Journey Toward Cure Rare Disease Foundation NFED

Standardizing Medical Interpretation of Genomics Data

Battle BPAN Warriors

Key Findings Genomic Landscape ALS

Mastermind: Comprehensive Genomic Association Search Engine

Comprehensive Genomic Landscape ALS

Novel PHEX Gene Locus‐Specific Database: Comprehensive Characterization Variants X‐linked Hypophosphatemia

Development Comprehensive, Locus-Specific Patient Database ENPP1 Deficiency

ENPP1 Deficiency: Clinical Update Relevance Individual Variants Locus-Specific Patient Database

Artificial Intelligence for Drug Discovery

Estimation ENPP1 Deficiency Genetic Prevalence

Estimation global prevalence PLA2G6-associated neurodegeneration

Clarification variant reporting homologous genes resolved systematic literature review

Genomic Landscape Rare Obesity Disorders

Intronic Variant Quick Reference

Mastermind Variant Interpretation Cards

Mastermind Variant Interpretation Poster

Genomenon and BeginNGS: The Promising Future of Newborn Sequencing

Mastermind Story Rare Genomics Institute

Mastermind Story Rady Childrens Institute for Genomic Medicine

Unraveling Genomic Complexity: Expert Insights Variant Curation Interpretation

Mastermind’s New ClinVar Integration Accelerate Clinical Diagnoses

Curating Human Genome Advance Early Identification Rare Diseases

Precision Medicine Roadmap Rx CDx Codevelopment Regulatory Approval Japan

ACMG 2024 Clinical Genetics Meeting Exhibit Theater Presentation

ACMG 2024 Clinical Genetics Meeting Scientific Platform Presentation

Interpreting Splice Variants: Contemporary Classification Tools and Methods

Developing Treatments for Rare Disease

Mastermind Masterclass: Gene Information Page

Leveraging Literature for Effective Variant Curation

Mastermind Evidence Page Overview

Mastermind Gene Page Overview

Launching a Search

Getting Started

Codon Charts

The End of VUS? Impact on Diagnosis and Treatment of Rare Diseases

Lurie Children's Hospital Case Study

The Genetic Code Beneath the Surface: Uncovering Melanoma’s Molecular Blueprint

RWE for Precision Medicine: A New Era of Genomic Intelligence in Drug Development

Fueling Discovery with Purpose: Free Variant Insights for 33 Clinically Significant Genes

Genomic Intelligence in Brain Cancer: From Curated Insights to Targeted Treatments

Introducing Mastermind CORE for genomic discovery

Mastermind CORE is a powerful research tool that lets users experience all the features that Mastermind PRO offers, with access to a select subset of the 19,000 genes.

Create an account and see how Mastermind can enhance your research!