Following clinical feedback, improvements have been made to several genomics forms. All updated forms are now available on the NHS England website: NHS England » Genomics resources.
Please note that issues have been identified when completing forms using a web browser or Outlook. For full functionality, please use Adobe Reader or Acrobat when accessing and completing genomics forms. Issues had also been identified when using an Apple Mac laptop, dropdown lists were randomly selecting other items on the list. A fix has been applied to the test order forms for Rare Disease and Cancer.
The changes align with the recent National Genomic Test Directory (NGTD) updates from 8th April and have been informed by extensive national consultation with requesting clinicians. A list of updated forms is as follows:
- Young Person Assent
- Consultee Declaration
- Record of Discussion:
- Changes have been made to the Record of Discussion form in English, Arabic, Bengali, Chinese, Gujarati, Polish, Portuguese, Punjabi, Spanish, Urdu, Welsh and Romanian
- Rare Disease Whole Genome Sequencing Test Order Form
- Please click here to read more on this
- This is for Whole Genome Sequencing in Rare Disease only; all referral forms can be seen by clicking here
- Cancer Whole Genome Sequencing Test Order Form
- This is for Whole Genome Sequencing in Cancer only; all referral forms can be seen by clicking here
- National Genomic Research Library Participant Leaflet
If there are any issues or queries please contact the Genomics Unit.