Find key test order forms, guidance documents and pathway guides for genomic tests available through the South West Genomic Medicine Service. This page is designed to help healthcare professionals quickly access the documents they need, but full guidance should always be read on the corresponding test or service page before completing a request.
Test Order Form library
GMS Test order form
Important
All samples for genomic testing should be accompanied by a fully completed request form.
- The request form should include as much clinical information about the patient or family member, family relationships and the requested test code (R number)
- All request forms must indicate either a specific disorder/gene(s) to be investigated or, a request to extract and store DNA
- This form should be used for the majority of test requests
- Please do not download and store this on your desktop or system. The form is regularly updated. Our recommendation is to save or bookmark a link to our website to ensure you are working with the most up-do-date version.
BHODS form
For full information, please visit the haematological malignancy testing page.
ctDNA test order form
The ctDNA service for the SW is provided by the Royal Marsden.
To request a ctDNA test, please e-mail Marsden360@rmh.nhs.uk for a Test Order Form.
For further guidance, please visit the ctDNA pages.
Sarcoma test order form
SWGLH-Sarcoma-Genomics-Test-Request-Form-access
For more information, please visit the Solid tumour test page.
Non-haematological tumours test order form
SWGLH- Cancer Genomics Test Request Form – Solid Tumour-Adult
For more information, please visit the Solid tumour test page.
Neurological tumours test order form
SWGLH- Neurological Tumours Request Form
For guidance, please visit the Solid Tumours test page
R454 Mavacamten test order form
GMS Test Order Form for R454 CYP2C19-Mavacamten
For guidance, please visit the Mavacamten testing page.
R14 - Rapid Whole Genome Testing Service test order form
Please visit the R14 pages for full guidance.
R14 reanalysis test request
Please visit the R14 pages for full guidance.
Whole Genome Sequencing for solid tumours in young people
- Please complete the two forms below and send to SWGLHexports@nbt.nhs.uk
- NHS Genomic Medicine Service test order form – Cancer
- NHS Genomic Medicine Service record of discussion form
Please visit the WGS for solid tumours in young people page for full guidance.
Whole Genome Sequencing (WGS) for solid tumours and sarcoma
- Please complete the two forms below and send to SWGLHexports@nbt.nhs.uk
- NHS Genomic Medicine Service test order form – Cancer
- NHS Genomic Medicine Service record of discussion form
Please visit the WGS for solid tumours and sarcoma page for full guidance.
Whole Genome Sequencing (WGS) for haematological malignancy
- Complete the two forms below and send to SWGLHexports@nbt.nhs.uk
- BHODS-form-v5-18092025
- NHS Genomic Medicine Service record of discussion form
Please visit the WGS for haematological malignancy page for full guidance.
Whole Genome Sequencing for Rare Disease
- To request a whole genome sequencing test for rare disease, you will need to download and complete the NHS WGS test order form for rare disease
- Please also complete the NHS Genomic Medicine Service Record of Discussion form.
- You will need to send these to: SWGLHexports@nbt.nhs.uk
Visit the WGS Rare Disease testing page for full guidance.
Consent forms and additional forms for patients library
Mainstreaming consent form
Germline genetic tests have implications for future and family health. Patients should be informed of the implications and be appropriately consented, using a tool such as the Mainstreaming Consent Form to document in the patient record.
Mainstreaming Consent form for Inherited Cancer
Please visit the inherited cancer testing pages for full guidance.
R14 Record of discussion form
Record_of_Discussion_regarding_R14_Rapid_Genome_Sequencing_v3.0
Please visit the R14 pages for full guidance.
WGS record of discussion form
WGS genomic consultee declaration
WGS young persons’ assent form
Participation in research form
Below is the form for opt in and out to the National Genomic Research Library as part of the WGS conversation process:
Pathway guides Library
One Page Guide for Rare Disease WGS Pathway
R14 workflow
WGS Cancer Pathway Sarcoma short guide
WGS Cancer Pathway Sarcoma short guide
Please visit the WGS for solid tumours and sarcoma page or the WGS for solid tumours in young people page for full guidance.
WGS Cancer Pathway under 25 short guide
WGS Cancer Pathway under 25 short guide
Please visit the WGS for solid tumours in young people page for full guidance.
WGS Cancer Pathway Haem Onc short guide
WGS Cancer Pathway Haem Onc short guide
Please visit the WGS for haematological malignancy page for full guidance.
WGS Cancer Pathway brain tissue short guide
WGS Cancer Pathway brain tissue short guide
Please visit the WGS for solid tumours in young people page for full guidance.
Breast R208 Overview guide
Breast R208 Overview FINAL v1.4 (2) (1)
Please visit the R208 page for full guidance.