Clinical Indication ID & Name
R375
Family follow-up testing to aid variant interpretation
Test Group
Core/Specialised
Specialties
Test code
R375.1
Test name
N/A
Target genes
Specific Target
Test scope
n/a
Test method/ technology
Targeted mutation testing
Optimal Family Structure
n/a
Eligibility Criteria
Family follow-up testing to aid variant interpretation
Commissioning group
Core/Specialised
Overlapping idications
n/a
Address for samples/request forms
North Thames GLH, Rare & Inherited Disease Genomic Laboratory
Specimen Reception, Level 5 Barclay House, 37 Queen Square,
London WC1N 3BH
Contact with queries
Supporting documents
Rare Disese WGS Clinician pack
Education resources
n/a
Service updates
n/a
Request form download
Consent record
See consent guidance in test request form
Sample requirements
See sample guidance in test request form