Identity testing
Clinical Genetic Test
Help
offered by
GTR Test Accession: Help GTR000558848.1
INHERITED DISEASE
Last updated in GTR: 2018-01-09
Last annual review date for the lab: 2021-12-28 Past due LinkOut
At a Glance
Diagnosis
Dizygotic twins
Chromosome 13; Chromosome 18; Chromosome 21; Sex chromosome X; Sex chromosome Y
Molecular Genetics - Targeted variant analysis: QF-PCR
Not provided
Not provided
Not provided
Ordering Information
Offered by: Help
Molecular Genetics Laboratory
Test service: Help
Identity Testing
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
Decline to answer
Post-test genetic counseling required: Help
Decline to answer
Recommended fields not provided:
Conditions Help
Total conditions: 1
Condition/Phenotype Identifier
Test Targets
Chromosomal regions/Mitochondria Help
Total chromosomal regions/mitochondria: 5
Chromosomal region/Mitochondrion Associated condition
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Targeted variant analysis
QF-PCR
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis
Recommended fields not provided:
Technical Information
Test Procedure: Help
STS markers on Chromosomes 13, 18, 21, X and Y
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
sensitivity: 100%; specficity: 100%
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
Recommended fields not provided:
Regulatory Approval
FDA Review: Help
Not provided
Additional Information

IMPORTANT NOTE: NIH does not independently verify information submitted to GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.