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

Von Willebrand disease (VWD) is a blood disorder in which the blood doesn't clot properly. Blood contains many proteins that help blood clot when needed. One such protein is called von Willebrand factor (VWF).


The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp

• Available in less than 24 hours
• Based on Whole Genome Sequencing
• More than 5 genes analyzed
• Investigates SNP and Indel mutations up to 150 bp

List of conditions:

• Von Willebrand

List of genes:

ADAMTS13, COL6A5, F8, GP1BA, GP1BB, GP9, VWA3B, VWF