PGx-Standard (Preemptive PGx test)
Clinical Genetic Test
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offered by
GTR Test Accession: Help GTR000597448.1
PHARMACOGENOMICINHERITED DISEASE
Last updated in GTR: 2022-04-27
Last annual review date for the lab: 2023-03-16 Past due LinkOut
At a Glance
Drug Response
Voriconazole response; Aspirin response; Azathioprine response more...
CYP2C19 (10q23.33); CYP2C9 (10q23.33); CYP2D6 (22q13.2); CYP3A5 (7q22.1); DPYD (1p21.3) more...
Molecular Genetics - Targeted variant analysis: SNP Detection
Available for all ethnicity and populations
Not provided
Not provided
Ordering Information
Offered by: Help
SPMED CO., LTD
View lab's website
Test Order Code: Help
SGH005_V2
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: 31
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 10
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
SNP Detection
* Instrument: Not provided
Clinical Information
Test purpose: Help
Drug Response
Target population: Help
Available for all ethnicity and populations
Recommended fields not provided:
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
SPMED PGx-Standard has more than 95% sensitivity (limit of detection), 100% sensitivity for the cut off value, 100% accuracy, 100% precision for repeatability and reproducibility and no cross-reactivity and interference regarding specificity.
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.