Clinical Genetic Test
offered by
GTR Test Accession:
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GTR000569434.4
CAP
Last updated in GTR:
2024-06-21
View version history
GTR000569434.4,
last updated:
2024-06-21
GTR000569434.3,
last updated:
2022-06-23
GTR000569434.2,
last updated:
2021-07-13
GTR000569434.1,
registered in GTR:
2019-10-30
Last annual review date for the lab: 2024-06-28
LinkOut
At a Glance
Test purpose:
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Drug Response;
Therapeutic management
Conditions (2):
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Ribavirin response;
Hepatitis C virus infection, response to therapy of
Genes (1):
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ITPA (20p13)
Methods (1):
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Molecular Genetics - Targeted variant analysis: SNP Detection
Target population: Help
Patients being treated or considering treatment with Ribavirin to assess …
Clinical validity:
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Not provided
Clinical utility:
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Not provided
Ordering Information
Offered by:
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Specimen Source:
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- Peripheral (whole) blood
- View specimen requirements
Who can order: Help
- Licensed Physician
Test Order Code:
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91416
View other test codes
View other test codes
CPT codes:
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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.
How to Order:
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4 ml whole blood collected in an EDTA (lavender-top ) tube
minimum 2 ml
minimum 2 ml
Informed consent required:
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Based on applicable state law
Pre-test genetic counseling required:
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No
Post-test genetic counseling required:
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No
Recommended fields not provided:
Lab contact for this test,
Test strategy,
Test development
Conditions
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Total conditions: 2
Condition/Phenotype | Identifier |
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Test Targets
Genes
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Total genes: 1
Gene | Associated Condition | Germline or Somatic | Allele (Lab-provided) | Variant in NCBI |
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Methodology
Total methods: 1
Method Category
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Test method
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Instrument *
Targeted variant analysis
SNP Detection
* Instrument: Not provided
Clinical Information
Test purpose:
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Drug Response;
Therapeutic management
Target population:
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Patients being treated or considering treatment with Ribavirin to assess risk of ribavirin induced anemia
Recommended fields not provided:
Clinical validity,
Clinical utility,
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
Test performance comments
San Juan Capistrano, Quest Diagnostics
Entire test performed in-house
Test performance comments
San Juan Capistrano, Quest Diagnostics
Analytical Validity:
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Sensitivity/specificity >99%
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 College of Medical Genetics / College of American Pathologists, ACMG/CAP
Yes
Method used for proficiency testing: Help
Formal PT program
PT Provider: Help
American College of Medical Genetics / College of American Pathologists, ACMG/CAP
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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Not provided
NYS CLEP Approval:
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Number:
32271
Status: Pending
Status: Pending
Additional Information
Reviews:
Clinical resources:
Molecular resources:
Consumer resources:
IMPORTANT NOTE:
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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.