Von Willebrand Report

 This product is only meant for customers who already 
purchased a Sequencing Test

The Von Willebrand Report is based on Whole Genome Sequencing Test. As such, it analyzes all Common and Rare Variants associated with Von Willebrand instead of a limited set of genes, like old genetic target panels.

Von Willebrand disease is a bleeding disorder that slows the blood clotting process, causing prolonged bleeding after an injury. People with this condition often experience easy bruising, long-lasting nosebleeds, and excessive bleeding or oozing following an injury, surgery, or dental work. Mild forms of Von Willebrand disease may become apparent only when abnormal bleeding occurs following surgery or a serious injury. Symptoms of Von Willebrand disease may change over time. Increased age, pregnancy, exercise, and stress may cause bleeding symptoms to become less frequent.

Along with environmental factors, Genetics plays a key role in the regulation of Von Willebrand.

 

• 9 genes analyzed
• 100% genomic regions covered
• Intragenic and intergenic regions analyzed
• All variants reported

 

 

List of genes:

GP1BA

VWF

ADAMTS13

GP9

GP1BB

VWA3B

COL6A5

F8