The Jackson Laboratory

Consumer Genomics Education

Consumer genomic testing has evolved rapidly since the first tests became available in the mid-2000s. Now individuals can access many types of genomic information on their own, without the guidance of their healthcare provider. This can include information that is potentially medically actionable. Clinical & Continuing Education at The Jackson Laboratory has several resources for you to understand this quickly evolving landscape, from online case-based learning to resources that will help you discuss findings and know when to order confirmatory testing in a clinical lab.

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Genomic Testing for the Healthy Individual

Genomic Testing for the Healthy Individual

Learn how to elicit patient motivations for genomic testing and to assess if a particular genomic test is a good fit for their concerns.

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Access CNE Module

Clinical Confirmation of Consumer Genetic Test Results Tile

Clinical Confirmation of Consumer Genetic Test Results

Helps clinicians recognize when consumer genomic test results should be clinically confirmed.

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Five Misconceptions About Consumer Genomic Testing

Five Misconceptions about Consumer Genomic Testing

Genomic testing in healthcare is here to stay. Use of testing is increasing, not only in the traditional sense (think hereditary cancer or prenatal genetics), but also outside the doctor’s office.

When Should You Seek Clinical Confirmation of Consumer Genomic Test Results?

When should you seek clinical confirmation of consumer genomic test results?

Why do millions of Americans and others around the world participate in consumer genomics? For many, testing provides a window into their innermost self, their genome...

Accessing Genetic Services

Accessing Genetic Services

Tool to help healthcare providers and patients find genetic services, including genetics providers, genetic testing and screening services.

GINA Discussion Guide

Genetic Information Nondiscrimination Act (GINA)

Provides information about the federal law that protects individuals from the misuse of genetic information in health insurance and employment.

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