Pancreatitis Panel
Clinical Genetic Test
Help
offered by
GTR Test Accession: Help GTR000560621.6
NYS CLEP
CAP
INHERITED DISEASERESPIRATORY DISEASEENDOCRINOLOGY ... View more
Last updated in GTR: 2023-03-28
Last annual review date for the lab: 2024-03-22 LinkOut
At a Glance
Diagnosis; Pre-symptomatic
Hereditary pancreatitis; Bronchiectasis with or without elevated sweat chloride 1; Congenital bilateral aplasia of vas deferens from CFTR mutation more...
Genes (6): Help
CASR (3q13.33-21.1); CFTR (7q31.2); CPA1 (7q32.2); CTRC (1p36.21); PRSS1 (7q34) more...
Molecular Genetics - Sequence analysis of the entire coding region: Next-Generation (NGS)/Massively parallel sequencing (MPS)
Not provided
Clinical validity depends on specific clinical and family history.
Not provided
Ordering Information
Offered by: Help
Specimen Source: Help
Who can order: Help
  • Genetic Counselor
  • Health Care Provider
  • Licensed Physician
  • Nurse Practitioner
Test Order Code: Help
8022
Lab contact: Help
Monalyn Salvador, MS, CGC, Manager, Product Management - Oncology
[email protected]
949-457-8961
How to Order: Help
Test service: Help
Clinical Testing/Confirmation of Mutations Identified Previously
    OrderCode: 5555
Test development: Help
Test developed by laboratory (no manufacturer test name)
Informed consent required: Help
Based on applicable state law
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: 6
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 6
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Sequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis; Pre-symptomatic
Clinical validity: Help
Clinical validity depends on specific clinical and family history.
Variant Interpretation:
Will the lab re-contact the ordering physician if variant interpretation changes? Help
Yes.
Recommended fields not provided:
Technical Information
Test Confirmation: Help
Single nucleotide variant calls not satisfying 100x depth of coverage and 40% het ratio thresholds are verified by Sanger sequencing (Mu W et al. J Mol Diagn. 2016 Oct 4. PubMed PMID: 27720647).
Test Comments: Help
Prenatal testing may be available. Please contact the lab for details.
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
This test is designed and validated to be capable of detecting >99% of described mutations in the gene(s) represented.
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:
Regulatory Approval
FDA Review: Help
Category: FDA exercises enforcement discretion
NYS CLEP Approval: Help
Number: 73884
Status: Approved
Additional Information

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