Clinical Genetic Test
offered by
GTR Test Accession:
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GTR000522604.10
Last updated in GTR:
2022-12-06
View version history
GTR000522604.10,
last updated:
2022-12-06
GTR000522604.9,
last updated:
2022-11-22
GTR000522604.8,
last updated:
2022-10-20
GTR000522604.7,
last updated:
2022-10-13
GTR000522604.6,
last updated:
2022-08-25
GTR000522604.5,
last updated:
2022-05-02
GTR000522604.4,
last updated:
2022-04-28
GTR000522604.3,
last updated:
2019-04-30
GTR000522604.2,
last updated:
2019-01-15
GTR000522604.1,
registered in GTR:
2018-05-18
Last annual review date for the lab: 2024-04-17
LinkOut
At a Glance
Methods (1):
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Molecular Genetics - Sequence analysis of the entire coding region: Next-Generation (NGS)/Massively parallel sequencing (MPS)
Target population: Help
Not provided
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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- Amniocytes
- Amniotic fluid
- Chorionic villi
- Cord blood
- Fibroblasts
- Fresh tissue
- Isolated DNA
- Peripheral (whole) blood
- Saliva
- Skin
Who can order: Help
- Health Care Provider
- Licensed Physician
Lab contact:
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Robin Fletcher, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
[email protected]
864-388-1055
Kellie Walden, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
[email protected]
334-246-3647
[email protected]
864-388-1055
Kellie Walden, MS, CGC, Certified Genetic counselor, CGC, Genetic Counselor
[email protected]
334-246-3647
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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Test service:
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Clinical Testing/Confirmation of Mutations Identified Previously
Test development:
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Test developed by laboratory but exempt from FDA oversight (eg. NYS CLEP approved, offered within a hospital or clinic)
Informed consent required:
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Decline to answer
Pre-test genetic counseling required:
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Decline to answer
Post-test genetic counseling required:
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Decline to answer
Recommended fields not provided:
Test Order Code,
Test strategy
Conditions
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Total conditions: 6
Condition/Phenotype | Identifier |
---|
Test Targets
Genes
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Total genes: 11
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 *
Sequence analysis of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
* Instrument: Not provided
Clinical Information
Test purpose:
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Diagnosis
Recommended fields not provided:
Clinical validity,
Clinical utility,
Target population,
What is the protocol for interpreting a variation as a VUS?,
Is research allowed on the sample after clinical testing is complete?,
Sample negative report,
Sample positive report
Technical Information
Test Comments:
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This panel is available for prenatal diagnosis in cases with suggestive ultrasound findings. Please contact the lab to discuss the case prior to sending a sample for prenatal analysis.
Availability:
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Tests performed
Entire test performed in-house
Entire test performed in-house
Analytical Validity:
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Sequence method detects 99% of sequence variants
Proficiency testing (PT):
Is proficiency testing performed for this test?
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Yes
Method used for proficiency testing: Help
Inter-Laboratory
Yes
Method used for proficiency testing: Help
Inter-Laboratory
Recommended fields not provided:
Test Confirmation,
Assay limitations,
Description of internal test validation method,
Citations for Analytical validity,
PT Provider,
Description of PT method,
Major CAP category, CAP category, CAP test list
Regulatory Approval
FDA Review:
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Not provided
Additional Information
Reviews:
Clinical resources:
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.