Clinical Indication ID & Name
R263
Confirmation of uniparental disomy
Test Group
Core/Specialised
Specialties
Test code
R263.1
Test name
N/A
Target genes
As relevant to clinical setting
Test scope
n/a
Test method/ technology
UPD testing
Optimal Family Structure
n/a
Eligibility Criteria
Confirmation of probable UPD identified by methylation testing at imprinted loci and UPD identified via other routes, for example SNP array, exome ore genome sequencing. This could include testing for mosaic genome-wide UPD
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