GTR Test Accession:
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GTR000569851.1
Registered in GTR:
2020-01-02
View version history
GTR000569851.1,
registered in GTR:
2020-01-02
Last annual review date for the lab: 2024-08-01
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At a Glance
Methods (2):
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Molecular Genetics - Sequence analysis of select exons: Sequence based typing (SBT); ...
Target population: Help
Not provided
Clinical validity:
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Not provided
Clinical utility:
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Not provided
Ordering Information
Offered by:
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HLA Laboratory
Specimen Source:
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- Peripheral (whole) blood
Who can order: Help
- Health Care Provider
- Licensed Physician
Contact Policy:
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Laboratory can only accept contact from health care providers. Patients/families are encouraged to discuss genetic testing options with their health care provider.
Test service:
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Histocompatability
Test development:
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FDA-reviewed (has FDA test name)
Informed consent required:
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Decline to answer
Pre-test genetic counseling required:
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Decline to answer
Post-test genetic counseling required:
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Decline to answer
Recommended fields not provided:
Test Order Code,
How to Order,
Lab contact for this test,
Test strategy
Conditions
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Total conditions: 1
Condition/Phenotype | Identifier |
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Test Targets
Genes
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Total genes: 6
Gene | Associated Condition | Germline or Somatic | Allele (Lab-provided) | Variant in NCBI |
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Methodology
Total methods: 2
Method Category
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Test method
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Instrument *
Sequence analysis of select exons
Sequence based typing (SBT)
Targeted variant analysis
Sequence specific oligonucleotide probe (SSOP, SSO)
* Instrument: Not provided
Clinical Information
Test purpose:
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Screening
Recommended fields not provided:
Clinical validity,
Clinical utility,
Target population,
What is the protocol for interpreting a variation as a VUS?,
Are family members with defined clinical status recruited to assess significance of VUS without charge?,
Will the lab re-contact the ordering physician if variant interpretation changes?,
Is research allowed on the sample after clinical testing is complete?,
Sample negative report,
Sample positive report
Technical Information
Availability:
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Tests performed
Entire test performed in-house
Entire test performed in-house
Analytical Validity:
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The SSO-CWD Test is an IVD approved test and validated in our laboratory using ASHI approved guidelines for HLA SSO based typing. 15 previously typed samples were tested at the A,B,C and DRB1 loci and compared to historic samples. The SSO-CWD typing was fully concordant with all evaluable genotypes in …
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Proficiency testing (PT):
Is proficiency testing performed for this test?
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Yes
Method used for proficiency testing: Help
Formal PT program
PT Provider: Help
American Society for Histocompatibility and Immunogenetics
Yes
Method used for proficiency testing: Help
Formal PT program
PT Provider: Help
American Society for Histocompatibility and Immunogenetics
Recommended fields not provided:
Test Confirmation,
Assay limitations,
Description of internal test validation method,
Citations for Analytical validity,
Description of PT method,
Major CAP category, CAP category, CAP test list
Regulatory Approval
FDA Review:
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Additional Information
Reviews:
Clinical resources:
Molecular resources:
Consumer resources:
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