Pancreatitis Panel
Clinical Genetic Test
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offered by
GTR Test Accession: Help GTR000569561.1
INHERITED DISEASEENDOCRINOLOGYIMMUNOLOGY ... View more
Last updated in GTR: 2019-11-15
At a Glance
Diagnosis
Neonatal severe primary hyperparathyroidism; Autosomal dominant hypocalcemia 1; Bronchiectasis with or without elevated sweat chloride 1; ...
Genes (6): Help
CASR (3q13.33-21.1), CFTR (7q31.2), CTSB (8p23.1), PRSS1 (7q34), SLC37A4 (11q23.3), ...
Molecular Genetics - Sequence analysis of the entire coding region: Next-Generation (NGS)/Massively parallel sequencing (MPS)
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Not provided
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Ordering Information
Offered by: Help
CNH Molecular Diagnostics Laboratory
View lab's website
Test Order Code: Help
MO0099
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: 13
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
Recommended fields not provided:
Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
The analytical sensitivity of NGS sequencing is estimated to be > 99% at detecting single nucleotide events. It will not reliably detect deletions greater than 20 base pairs, insertions or rearrangements greater than 10 base pairs, or low-level mosaicism.
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

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