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CYP2C9 genotyping
Clinical Genetic Test
Help
offered by
Sinochips Diagnostics
GTR Test Accession: Help GTR000592428.1
CAP
PHARMACOGENOMICINHERITED DISEASE
Last updated in GTR: 2021-02-15
View version history
Last annual review date for the lab: 2024-01-01 LinkOut
At a Glance
Test purpose: Help
Risk Assessment; Monitoring; Drug Response; ...
Conditions (11): Help
Phenytoin response; Celecoxib response; Flurbiprofen response; ...
Genes (2): Help
CYP2C9 (10q23.33), VKORC1 (16p11.2)
Methods (1): Help
Molecular Genetics - Targeted variant analysis: RT-PCR
Target population: Help
Not provided
Clinical validity: Help
Not provided
Clinical utility: Help
Not provided
Ordering Information
Offered by: Help
Sinochips Diagnostics
View lab's website
Test short name: Help
CYP2C9
Specimen Source: Help
Who can order: Help
  • Registered Nurse
  • Out-of-State Patients
  • Physician Assistant
  • Genetic Counselor
  • Health Care Provider
  • In-State Patients
  • Nurse Practitioner
  • Licensed Physician
  • Public Health Mandate
Contact Policy: Help
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: Help
Please fill in the contact form at https://sinochipsdiagnostics.com/contact/ or give us a call (877) 746-6244.
Order URL
Test development: Help
Test developed by laboratory (no manufacturer test name)
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:
Test Order Code, Lab contact for this test, Test strategy
Conditions Help
Total conditions: 11
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 2
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Targeted variant analysis
RT-PCR
* Instrument: Not provided
Clinical Information
Test purpose: Help
Risk Assessment; Monitoring; Drug Response; Therapeutic management
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: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Accuracy 97.4%; analytical Sensitivity 3.1 ng/uL; precision 96.7%
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
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: Help
Not provided
Additional Information
Consumer resources:

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.