Cardio IQ® 4q25-AF Risk Genotype
Test code
CPT code(s)*
Test resources
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Details
Methodology
Real-Time Polymerase Chain Reaction (PCR)
Assay category
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.
Alternative name(s)
Atrial Fibrillation (AF),CardioIQ®,4q25-AF Risk Genotype,rs10033464,rs2200733
Specimen requirements | |
|---|---|
| Patient preparation | None Specified |
| Preferred specimen(s) | 4 mL whole blood collected in an EDTA (lavender-top) tube |
| Minimum volume | 2 mL |
| Collection 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 container | EDTA (lavender-top) tube |
| Transport temperature | Refrigerated (cold packs) |
| Specimen stability | Room temperature: 8 days Refrigerated: 8 days Frozen: 30 days |
Reference ranges are provided as general guidance only. To interpret test results use the reference range in the laboratory report.
*The CPT codes provided are based on AMA guidance and are for informational purposes only. CPT coding is the sole responsibility of the billing party. Please direct any questions regarding coding to the payer being billed.
This material contains content from LOINC® (http://loinc.org). The LOINC Table, LOINC Table Core are copyright © 1995-2019, Regenstrief Institute, Inc. and the Logical Observation Identifiers Names and Codes (LOINC) Committee and is available at no cost under the license at http://loinc.org/license.
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