von Willebrand Disease (VWF) sequencing
von Willebrand Disease (VWF) sequencing-994
von Willebrand factor deficiency
VWD type 1
VWD type 2
VWD type 2A
VWD type 2M
VWD type 3
VWD type B
VWF gene
- Molecular test to confirm a phenotypic diagnosis of von Willebrand disease (VWD) types 1, 2A, 2B, 2M, 2N, or 3.
- May also be used as carrier screening for autosomal recessive forms of VWD.
Immediately following collection, mix sample thoroughly by gently inverting 8 - 10, times to prevent clotting
Lavender (EDTA), 4mL
Yellow ACD (A or B)
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.
Refrigerated (preferred) - 2 weeks
Ambient – 72 hours
Frozen – NO
- Serum or plasma
- Grossly hemolyzed specimens
- Frozen specimens
Massively Parallel Sequencing
See report
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.