Genetics in primary care - "...we should be seeking advice about that family history"

Dr Jude Hayward, GP in Bradford and GPwSI in Genetics with the Yorkshire Regional Genetics Service, joins GPs Rebecca and Sarah to break down the essentials of genomics and genetic testing in primary care. This episode covers key terminology, like germline and somatic variants, the practical role of family history in identifying inherited cancer risk, when to refer to genetics services and the impact of targeted therapies in modern cancer care. Plus, learn how to support patients navigating genetic results and hear about evolving guidance and resources to empower GPs in personalised and precision medicine.Recommended cancer key article: Clinical genetic referrals: a practical guide for primary care If you loved this episode and would like to hear more like this, please send your review to [email protected] and share the series with a colleague.GPs Talk Cancer is the podcast series from GatewayC. GatewayC is the free early cancer diagnosis resource funded by the NHS and is part of The Christie NHS Foundation Trust. View the full shownotes for this episode at Podcast - GatewayCProduced by GatewayC and Listening Dog Media.DISCLAIMER: We know this podcast might be of interest to anybody, however it is aimed at primary care health professionals. All patient cases are based on real stories from our clinical practice as GPs. They are fully anonymised with no identifiable patient data. All featured statistics are accurate at the time of recording. All views expressed by guest speakers are their own. Hosted on Acast. See acast.com/privacy for more information.