Healthcare Provider Genomics Education Resources
Healthcare providers (HCPs) will increasingly use knowledge about genomics to meet the needs of their patients. This page provides resources targeted to HCPs and their educators.
Healthcare Professionals' Genomics Education Week
Building on the success of the 2021 social media campaign, NHGRI is planning another event from June 6-10, 2022, focusing on healthcare provider genomics education resource dissemination.
General Genomics Education Resources
Global Genetics and Genomics Community (G3C): Collection of unfolding video genetic and genomic case studies for use with students and practicing healthcare providers learning basic genetic and genomic concepts.
- Breast cancer risk assessment in an African American female: Grace
- Male breast cancer risk analysis in a Caucasian male: Jeff with wife Maria
- Colon cancer screening in a Hispanic male: Luis
- Familial adenomatous polyposis testing in an Ashkenazi Jewish male: Gabe
- Cancer screening incidental findings in an African American male with lung cancer: Tom
- Cardiovascular disease and diabetes risk in an adult Native American female: Lena
- Heart attack risk in an adult Puerto Rican female: Maria
- Hypercholesterolemia risk in an adult Hispanic female: Larissa
- Arrhythmia evaluation and cytochrome P450 enzyme CYP2C9 plus enzyme VKORC1 testing to guide treatment in an Ashkenazi Jewish male: Gabe #2
- Venous thromboembolism risk evaluation and cytochrome P450 enzyme CYP2C9 plus enzyme VKORC1 testing to guide treatment in an adult Caucasian female: Jennifer
- CYP2C19 testing in an adult African American male: Larry
- Opioid adverse reaction management of an African American child: Stephanie
- CYP2C19 testing in a Caucasian female for depression treatment selection: Carla
- Post-traumatic stress disorder in an adult Puerto Rican female: Peggy
- Newborn screening in an older pregnant Asian female: Day
- Cystic fibrosis risk in a pregnant Caucasian female: Lisa
- Sickle cell trait testing in a Caucasian male: Lucas
Direct-to-Consumer Genetic Testing
Direct-to-Consumer Genetic Testing FAQ for Healthcare Professionals
The Direct-to-Consumer Genetic Testing (DTC-GT) Project Group of the Inter-Society Coordinating Committee for Practitioner Education in Genomics (ISCC-PEG) has created a Frequently Asked Questions (FAQ) resource designed for the general clinician who may see patients requesting guidance on DTC-GT.
This FAQ is intended to help healthcare professionals understand the diverse landscape of DTC-GT, the benefits and limitations of these tests and how results of DTC-GT may affect their patients’ health, wellness and medical decision making.
Educational resources and learning modules for healthcare professionals on optimizing prescribing through the use of pharmacogenomics.
Pharmacogenomics Educational Links
- Clinical Pharmacogenetics Implementation Consortium (CPIC®): provides expert reviewed guidelines for drug-gene pair implementation, standardized terminology, amongst other resources.
- PharmGKB: google-like pharmacogenetic database which allows clinicians, students and researchers to search for pharmacogenetic information on drugs, genes, variants, regulatory resources and implementation resources.
- The Pharmacogenomics Global Research Network (PGRN): hosts weekly seminars on PGx research, implementation, and global PGx efforts. PGRN hosts an annual meeting allowing those interested in PGx to learn cutting edge science in the field.
Patient Care Resources
Tools for Collecting Family History
- My Family Health Portrait
Web-based tool to create a family pedigree with health information for patients and their providers to identify patterns of inheritance and identify risk factors.
- NHGRI’s Family Health History Resources
Locating a Genetics Clinic and Genetics Health Professionals
Clinical Trials Resources
- National Institutes of Health Clinical Trials
- National Institutes of Health, Clinical Center
- Clinical Research
- Current NHGRI Clinical Studies
Information About Specific Diseases
Clinical Research Resources
- Clinical Genome Resource (ClinGen): Resource that collects phenotypic and clinical information on variants across the genome, develops consensus approaches to identifying their clinical relevance and disseminates this information to researchers and clinicians. It will advance genomics in clinical care and improve our understanding of the phenotypic and functional effects of genetic variants and their clinical value.
- Omics Nursing Science & Education Network (ONSEN): Collaborative research and training website.
- Guide to Interpreting Genomic Reports: A Genomics Toolkit (CSER Consortium; February 2017): Guide for non-genetics practitioners to explain the different types of data found in whole genome sequencing or whole exome sequencing test reports, created by the Practitioner Education Working Group of the NHGRI Clinical Sequencing Exploratory Research consortium. It explains different categories in the test report (diagnostic, incidental or carrier) and provides next steps. There is also an embedded glossary of genomic terms.
Last updated: June 29, 2022