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Cardio IQ® APOE Genotype
Test Code90649
CPT Codes
81401
Preferred Specimen
4 mL whole blood collected in an EDTA (lavender-top) tube
Minimum Volume
2 mL
Instructions
Multiple (up to 8) cardiovascular-related genetic tests can be performed on a single specimen. A second EDTA (lavender-top) tube is required if non-genetic tests are simultaneously ordered that require an EDTA (lavender-top) tube. For whole blood samples, follow normal phlebotomy procedures.
Transport Temperature
Refrigerated (cold packs)
Specimen Stability
Room temperature: 8 days
Refrigerated: 8 days
Frozen: 30 days
Refrigerated: 8 days
Frozen: 30 days
Methodology
Real-Time Polymerase Chain Reaction (PCR)
FDA Status
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
Setup Schedule
Set up: Mon, Wed-Sat a.m.; Report available: 3-5 days
Reference Range
See Laboratory Report
Clinical Significance
This test determines the subtypes of APOE which will aid in the risk assessment of Coronary Heart Disease (CHD) and Hyperlipoproteinemia.