 |
|
Genetic Hypercoagulability Panel |
|
This panel tests for several significant single nucleotide polymorphisms associated with thrombosis.
|
|
|
|
| Factor V Leiden Mutation (G1691A) |
| MTHFR (C677T) Mutation |
| MTHFR (A1298C) Mutation |
| Prothrombin Mutation (G20210A) |
Preferred #
of Aliquots |
Volume
per Aliquot |
Preferred
Sample Type |
Processing |
Sample Source |
| 2 |
5mL
|
EDTA Whole Blood |
None |
|
|
|
|
|
|
©
2010 Machaon Diagnostics, Inc.
