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Genomics and personalised medicine

Explore more targeted care alongside uncertainty, family implications and fair access.

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By · Reviewed

Understand the topic

Genomic information can help explain some conditions and inform treatment choices. A genetic result may have uncertain significance, and risk is not always destiny. Results can also raise questions for relatives, creating consent and confidentiality considerations beyond the person tested.

How to discuss it in Med interview

Ask what the test can reliably tell us and how it would change care. Discuss informed consent, counselling, unexpected findings, data protection and access to follow-up. Consider whether evidence represents diverse populations and whether services can support people who receive uncertain results.

Put it into words

Before offering a genomic test, I would want the person to understand possible useful findings, uncertain findings and information they may not have expected. Specialist support can help them decide what information they want and how to discuss relevant findings with relatives.

Common pitfalls

Treating every variant as a diagnosis, assuming a result predicts the future with certainty or ignoring the person's preferences about information.

Official sources and further reading

Reviewed 2026-09-08. Check the linked guidance for changes before discussing current policy or law.