Factor ll gene mutation (evaluate Thrombophilia)
Factor ll gene mutation (evaluate Thrombophilia)-2260
Prothrombin
Prothrombin 20210 A
G20210A
Thrombin
F2
Detection of a point mutation (G to A at position 20210) of the human Factor II gene.
Clinically indicated for patients with personal or family history of thrombosis (especially venous) or risk factors of thrombosis.
- Only one (1) tube needs to be drawn for any combination of the following tests:
- Calreticulin Exon 9 Assay
- Factor V Leiden Mutation
- Factor 2 Mutation
- Hereditary Hemochromatosis
- JAK2 V617F Mutation Detection
- MTHFR C677T assay
- Immediately following collection, mix sample thoroughly by gentle inverting 8 - 10 times, to prevent clotting
Submit tube unspun
Lavender (EDTA), 4mL
Sodium citrate (Na cit) whole blood
Lt blue Sodium citrate (NaCit)
Yellow ACD (A or B)
Molecular Medicare billing request
Hospital clients submitting a request for this assay on an outpatient with Medicare should complete and submit a Molecular Medicare billing request form to notify us of the need for Allina Health Laboratory to bill insurance.
Ambient (preferred)
Refrigerated
- Improper label (unlabeled or mislabeled)
- Wrong container (anticoagulant or solution)
- Improper blood/anticoagulant ratio
- Delay in transport
- Improper storage
- Inappropriate timing of collection
- Interfering substances
- Leaking container
- Slides broken beyond repair
Cobas Factor II and Factor V Test
Homozygous normal
Hospital clients submitting a request for this assay on an outpatient with Medicare should complete and submit a Molecular Medicare billing request form to notify us of the need for Allina Health Laboratory to bill insurance.