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Pharmacogenomics SNaP-Shot
Clinical Genetic Test
Help
offered by
Ariel Precision Medicine
View lab's test page
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GTR Test Accession: Help GTR000593051.4
Last updated in GTR: 2023-08-16
View version history
Last annual review date for the lab: 2023-08-23 LinkOut
At a Glance
Test purpose: Help
Drug Response; Monitoring; Predictive; ...
Conditions (1): Help
Drug metabolism or response
Genes (26): Help
ABCG2 (4q22.1), ADRB1 (10q25.3), BCHE (3q26.1), CACNA1S (1q32.1), COMT (22q11.21), ...
Methods (1): Help
Molecular Genetics - Targeted variant analysis: SNP Detection
Target population: Help
Not provided
Clinical validity: Help
Not provided
Clinical utility: Help
Guidance for selecting a drug therapy and/or dose
Ordering Information
Offered by: Help
Ariel Precision Medicine
View lab's website
View lab's test page
Test short name: Help
Snapshot PGx
Specimen Source: Help
Who can order: Help
  • Genetic Counselor
  • Health Care Provider
  • Licensed Physician
  • Nurse Practitioner
  • Physician Assistant
Lab contact: Help
David Finegold, MD, ABMGG Board Certified, ABP, Diplomate of the American Board of M, Lab Director
info@arielmedicine.com
(844) 692-7435
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
1) Licensed clinician logs in to Ariel's secure portal via website
Order URL
Test service: Help
Clinical Testing/Confirmation of Mutations Identified Previously
Result interpretation
Test development: Help
Test developed by laboratory (no manufacturer test name)
Informed consent required: Help
Yes
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, Test strategy
Conditions Help
Total conditions: 1
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 26
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; Monitoring; Predictive; Therapeutic management
Clinical utility: Help
Guidance for selecting a drug therapy and/or dose
View citations (2)

Variant Interpretation:
Will the lab re-contact the ordering physician if variant interpretation changes? Help
Yes.
Research:
Is research allowed on the sample after clinical testing is complete? Help
Yes, but patient must provide consent to enable such activities.
Recommended fields not provided:
Clinical validity, 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?, Sample negative report, Sample positive report
Technical Information
Test Confirmation: Help
Confirmatory Sequencing
Availability: Help
Tests performed
Interpretation performed in-house
Report generated in-house
Specimen preparation performed both in-house and at an outside lab
Wet lab work performed at an outside lab

Test performance comments
Wet lab work is performed at partner laboratory. All elements of test performance characteristics were performed at the outside laboratory. Interpretation and report generation is performed in-house.
Analytical Validity: Help
The test demonstrates >98% analytical sensitivity and specificity for the variants tested.
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No

Method used for proficiency testing: Help
Intra-Laboratory
Recommended fields not provided:
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: 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.