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PGS.pharma
Clinical Genetic Test
Help
offered by
MVZ diagnosticum Frankfurt
GTR Test Accession: Help GTR000576338.1
INHERITED DISEASEPHARMACOGENOMICHEMATOLOGY ... View more
Registered in GTR: 2020-04-07
View version history
Last annual review date for the lab: 2024-06-07 LinkOut
At a Glance
Test purpose: Help
Drug Response
Conditions (18): Help
Angiotensin i-converting enzyme, benign serum increase; Beta-2-adrenoreceptor agonist, reduced response to; CYP2C19-related poor drug metabolism more...
Genes (12): Help
ACE (17q23.3); ADRB2 (5q32); COMT (22q11.21); CYP2C19 (10q23.33); CYP2C9 (10q23.33) more...
Methods (1): Help
Molecular Genetics - Targeted variant analysis: Allele-specific PCR
Target population: Help
Not provided
Clinical validity: Help
Not provided
Clinical utility: Help
Not provided
Ordering Information
Offered by: Help
MVZ diagnosticum Frankfurt
View lab's website
Specimen Source: Help
  • Buccal swab
  • Cell-free DNA
  • Isolated DNA
  • ETDA blood
  • Saliva
  • Sputum
Who can order: Help
  • Licensed Physician
Lab contact: Help
Daniela Steinberger, MD, Medical Director
cs@genetik.diagnosticum.eu
+49 695308437-0
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
Please check the website for test ordering
Order URL
Test service: Help
Clinical Testing/Confirmation of Mutations Identified Previously
Confirmation of research findings
Custom Balanced Chromosome Rearrangement Studies
Custom Deletion/Duplication Testing
Custom Sequence Analysis
Genetic counseling
Marker Chromosome Identification
Maternal cell contamination study (MCC)
Whole Exome Sequencing
Clinical Exome
Result interpretation
Uniparental Disomy (UPD) Testing
Test additional service: Help
Custom Prenatal Testing
Custom mutation-specific/Carrier testing
Test development: Help
Test developed by laboratory (no manufacturer test name)
Informed consent required: Help
Yes
Pre-test genetic counseling required: Help
No
Post-test genetic counseling required: Help
No
Recommended fields not provided:
Test Order Code, Test strategy
Conditions Help
Total conditions: 18
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 12
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
Allele-specific PCR
* Instrument: Not provided
Clinical Information
Test purpose: Help
Drug Response
Recommended fields not provided:
Clinical validity, Clinical utility, 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?, Will the lab re-contact the ordering physician if variant interpretation changes?, Is research allowed on the sample after clinical testing is complete?, Sample negative report, Sample positive report
Technical Information
Test Platform:
LGC KASP Genotyping
Availability: Help
Tests performed
Interpretation performed in-house
Report generated in-house
Specimen preparation performed in-house
Wet lab work performed in-house
Analytical Validity: Help
Not Provided, on demand (n=20)
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
No
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: Help
Category: Not Applicable
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.