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Factor V (Leiden) Mutation Analysis : 17900
Test CodeF5LQ or 17900
CPT Codes
81241
Transport Container
Preferred Specimen: 5 mL whole blood collected in an EDTA (lavender-top) tube
Alternative Specimens: Whole blood collected in EDTA (royal blue-top), sodium heparin (green-top), ACD solution A or B (yellow-top) tube, or lithium heparin (green-top)
Minimum Volume: 3 mL
Alternative Specimens: Whole blood collected in EDTA (royal blue-top), sodium heparin (green-top), ACD solution A or B (yellow-top) tube, or lithium heparin (green-top)
Minimum Volume: 3 mL
Transport Temperature
Room temperature.
Specimen Stability
Room temperature: 8 days; Refrigerated: 8 days; Frozen: 30 days
Methodology
Polymerase Chain Reaction and Detection
Setup Schedule
Sunday - Saturday
Report Available
3-5 days (From receipt at performing laboratory)
Limitations
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.
Reference Range
By report.
Clinical Significance
Factor V (Leiden) Mutation is a point mutation that causes resistance of Factor V protein degradation by activated protein C (APC). This mutation is associated with increased risk of venous thrombosis.
Performing Laboratory
Quest Diagnostics
