Resources for Participants and Providers

The IMAGINE Research Program is committed to empowering both participants and healthcare providers with the information they need to understand the results of genomic testing. The links on this page include trusted, easy-to-understand educational resources that may help you explore: 

  • The meaning of your results 
  • Common genetic conditions and risk factors 
  • Inheritance and family implications 
  • Guidelines for providers interpreting genetic findings 

These materials are not a substitute for medical advice but are provided to support meaningful conversations between participants and their care teams. We encourage you to reach out to the IMAGINE team or your healthcare provider with any questions.

For Participants and Families

MedlinePlus Genetics

A trusted resource to learn about genetics and your health. 
Developed by the U.S. National Library of Medicine, this site offers easy-to-understand information about genetic conditions, genes, testing, and inheritance. 

ACMG Secondary Findings (ClinVar)

Learn which genes are included in the ACMG list for clinically actionable findings—used to guide result return even if unrelated to the original reason for testing.

Pharmacogenomics Fact Sheet (Genome.gov)

Pharmacogenomics is the study of how your genes affect the way your body responds to medicines. This fact sheet from Genome.gov explains how genetic testing can help doctors choose the right medication and dose for you—making treatment safer and more effective.  

For Physicians and Providers

GeneReviews® – NCBI Bookshelf

An expert-reviewed, searchable reference for clinicians. GeneReviews provides peer-reviewed articles about inherited conditions, including diagnosis, management, and genetic counseling guidance.

CPIC Genes-Drug Guidelines

The Clinical Pharmacogenetic Implementation Consortium (CPIC) Genes–Drugs page provides evidence-based guidance on how genetic test results can be used to optimize medication selection and dosing for specific gene–drug pairs. It is a trusted resource for clinicians interpreting pharmacogenomic results, including many commonly prescribed medications.