We have published a range of resources on genomics:

Published documents

• NHS Genomic Medicine Service Test order form – Cancer – July 2022, v1.18
• NHS Genomic Medicine Service Test order form – Rare disease – August 2021, v1.2
• NHS Genomic Medicine Service record of discussion form – v4.03
• NHS Genomic Medicine Service genomic consultee declaration – v3.02
• NHS Genomic Medicine Service participation in research form – v2.02
• NHS Genomic Medicine Service participation in research leaflet – v1.4
• NHS Genomic Medicine Service Withdrawal from the National Genomic Research Library
• NHS Genomic Medicine Service young persons’ assent form – v3.02
• Implementing Lynch syndrome testing and surveillance pathways – 27 July 2021
• Guidance – Rapid exome sequencing service for fetal anomalies testing – July 2021
• Genomic Medicine Service alliances and the role of nurses and midwives within the new structure: Update for Chief Nurses and Heads of Midwifery – July 2020
• Genomic Medicine Service alliances and the role of pharmacy within the new structure: Update for hospital chief pharmacist and CCG lead pharmacists – July 2020
• NHS England Strategy: Improving Outcomes through Personalised Medicine – 7 September 2016

Whole genome sequencing patient information leaflets

• Whole genome sequencing for children: An information guide for parents, carers and families (www.cclg.org.uk)  – December 2022
• Whole genome sequencing for suspected cancer: Information for patients and family members – July 2021
• Patient information for cancer – easy read – July 2021
• Whole genome sequencing for a rare disease: Information for patients and family members – July 2021
• Patient information for rare disease – easy read – July 2021

Useful links

• Genomics England
• HEE Genomics Education Programme

Contact

If you have any questions about the NHS Genomic Medicine Service, please email us at england.genomics@nhs.net