Factor V Leiden Mutation Analysis

The common Factor V Leiden mutation, c.1691G>A (p.R506Q), causes autosomal dominant thrombotic tendency and resistance to activated protein C (APC). More than 90% of APC-resistant individuals have this specific mutation. This test neither explores the possibility of a mutation in another region of the gene nor tests for mutations in other genes that may be risk factors for the disease(s) seen in this patient. This laboratory performs targeted mutation analysis for p.R506Q.

Forms & Docs

Ordering

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Test Code
T0423

Turn Around Time
2-3 weeks

Billing

CPT Code
81241×1

Ordering Guidance

If there are questions regarding this test, please contact Client Services at 617-553-5880 or clientservices@claritasgenomics.com

Details

Genes Covered
F5, c.1691G>A

Methods
Sanger