GenepoweRx_Cardiac Care
Clinical Genetic Test
offered by
GTR Test Accession: Help GTR000607941.1
Last updated in GTR: 2023-07-20
Last annual review date for the lab: 2023-05-19 Past due LinkOut
At a Glance
Diagnosis; Mutation Confirmation; Pre-symptomatic; ...
Coronary artery disease, autosomal dominant, 1; Atrial fibrillation, familial, 1; Atrial fibrillation, familial, 10; ...
ABCA1 (9q31.1), ABCC9 (12p12.1), ACTC1 (15q14), ACTN2 (1q43), AKAP9 (7q21.2), ...
Molecular Genetics - Deletion/duplication analysis: Next-Generation (NGS)/Massively parallel sequencing (MPS); ...
Individuals with clinical symptoms consistent with Coronary artery disease risk, …
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Ordering Information
Offered by: Help
Test Order Code: Help
Informed consent required: Help
Decline to answer
Pre-test genetic counseling required: Help
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Post-test genetic counseling required: Help
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Conditions Help
Total conditions: 63
Condition/Phenotype Identifier
Test Targets
Genes Help
Total genes: 102
Gene Associated Condition Germline or Somatic Allele (Lab-provided) Variant in NCBI
Total methods: 4
Method Category Help
Test method Help
Instrument *
Deletion/duplication analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
Detection of homozygosity
Oligonucleotide hybridization-based DNA sequencing
Mutation scanning of the entire coding region
Next-Generation (NGS)/Massively parallel sequencing (MPS)
Targeted variant analysis
Next-Generation (NGS)/Massively parallel sequencing (MPS)
* Instrument: Not provided
Clinical Information
Test purpose: Help
Diagnosis; Mutation Confirmation; Pre-symptomatic; Prognostic; Risk Assessment; Screening; Therapeutic management
Target population: Help
Individuals with clinical symptoms consistent with Coronary artery disease risk, Hypertrophic cardiomyopathy risk, Arrhythmia, Brugada Syndrome, Atrial fibrillation, Long QT syndrome, Ventricular Arrhythmia, Cardiac Channelopathies, Familial Hypercholesterolemia or individuals with distorted lifestyle factors
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Technical Information
Availability: Help
Tests performed
Entire test performed in-house
Analytical Validity: Help
Repeatability and reproducibility of alterations associated with this test were evaluated. The results confirmed that the test is robust regarding repeatability and reproducibility of variant calling. Across all samples, the pre-sequencing process failure was ≤ 1%. All variants from all samples were consistent by 99.9%.
Proficiency testing (PT):
Is proficiency testing performed for this test? Help
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Regulatory Approval
FDA Review: Help
Not provided
Additional Information

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