Test Code FVDNA FACTOR V LEIDEN MUTATION, BLOOD
Additional Codes
Software | Test Code |
---|---|
Label Text | FVDNA |
EPIC | LAB10246 |
Performing Laboratory
NorDx Laboratories
Useful For
Coagulation disorders and to determine Zygosity
Method Name
Polymerase Chain Reaction (PCR) with DNA probes
This assay is a lab developed test established by the NorDx Molecular Pathology Laboratory. This laboratory is certified under the Clinical Laboratory Improvement Amendments (CLIA) as qualified to perform high complexity clinical laboratory testing. This test is used for clinical purposes. It should not be regarded as investigational or for research.
Reference Values
Negative (reported as negative or positive with zygosity)
Days and Times Test Performed
Wednesday
Evenings
Report Available
1 Day
Specimen Type
Whole Blood
Preferred Container
Lavender Top Tube (EDTA)
Preferred Volume
Whole Blood: 4.0 mL (Lavender Top Tube (EDTA))
Minimum Volume
Whole Blood: 0.5 mL (Lavender Top Tube (EDTA))
Specimen Collection and Handling
1. Sample must arrive within 7 days of collection.
2. Send at ambient temperature or refrigerated.
Specimen Stability Information
Specimen Type: Whole Blood
Refrigerated: 7 Days
Room Temp: 7 Days
Add On Capable
Yes
Advance Beneficiary Notice Requirements
This test, when ordered on Medicare patients, is subject to the National Coverage Determination (NCD) policies. Please verify that the diagnosis code (ICD code) you have chosen demonstrates medical necessity for the test as documented in the physician’s patient record. The CMS web site is available to assist you with this verification. A properly executed Advance Beneficiary Notice (ABN) must be submitted with the specimen if medical necessity is not demonstrated by the ICD code chosen.
CPT Code Information
CPT Code |
CPT Description |
CPT Disclaimer |
---|---|---|
81241 | F5 (Coagulation Factor V) Gene Analysis, Leiden Variant |
Keywords
FACTOR V LEIDEN
FV (FACTOR V)
FV (FACTOR V) GENE MUTATION
LEIDEN GENE
Performing Laboratory Location
NorDx Laboratories
Maximum Laboratory Time
8 Days
LOINC Code Information
21667-1
Clinical Significance
This test is will include a pathologist interpretation. The physician professional component will be billed separately by the consulting physician.