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BM Engraftment Mini
Clinical Genetic Test
Help
offered by
Allogen Laboratories-Cleveland Clinic
GTR Test Accession: Help GTR000569604.2
CANCERHEMATOLOGYINHERITED DISEASE ... View more
Last updated in GTR: 2019-12-05
View version history
Last annual review date for the lab: 2023-09-20 LinkOut
At a Glance
Test purpose: Help
Therapeutic management
Conditions (7): Help
Acute lymphoid leukemia; B-cell chronic lymphocytic leukemia; Chronic myelogenous leukemia, BCR-ABL1 positive; ...
Chromosomal regions/ Mitochondria (3): Help
D8S1179, D13S317, D16S539, D18S51, D21S11, D10S1248, D22S1045, D2S441, D1S1656, D12S391, D2S1338, D19S433; Penta D and Penta E plus Amelogenin; chromosomal region/mitochondrion: STR lOCI: CSF1PO, FGA, TH01, TPOX, vWA, D3S1358, D5S818, D7S820
Methods (1): Help
Molecular Genetics - Targeted variant analysis: STR Chimerism Anlysis
Target population: Help
Not provided
Clinical validity: Help
Not provided
Clinical utility: Help
Not provided
Ordering Information
Offered by: Help
Allogen Laboratories-Cleveland Clinic
Test short name: Help
BMEMA2
Specimen Source: Help
Who can order: Help
  • Health Care Provider
Test Order Code: Help
BMEMA2
CPT codes: Help
**AMA CPT codes notice

Copyright: 2023 American Medical Association. All rights reserved.

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
This test can be ordered through Cleveland Clinic Electronic Medical Record-EPIC.
Test service: Help
Histocompatibility
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:
Lab contact for this test, Test strategy, Test development
Conditions Help
Total conditions: 7
Condition/Phenotype Identifier
Test Targets
Chromosomal regions/Mitochondria Help
Total chromosomal regions/mitochondria: 3
Chromosomal region/Mitochondrion Associated condition
Methodology
Total methods: 1
Method Category Help
Test method Help
Instrument *
Targeted variant analysis
STR Chimerism Anlysis
* Instrument: Not provided
Clinical Information
Test purpose: Help
Therapeutic management
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 Procedure: Help
STR Genotypes of Bone Marrow/PBSC Recipient and Bone Marrow/PBSC Donor
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
>95% STR genotype performed
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
Yes

Method used for proficiency testing: Help
Formal PT program

PT Provider: Help
ASHI-American Society for Histocompatibility and Immunogenetics
Recommended fields not provided:
Test Confirmation, Assay limitations, Description of internal test validation method, Citations for Analytical validity, Description of PT method, Major CAP category, CAP category, CAP test list
Regulatory Approval
FDA Review: Help
Not provided
Additional Information

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.