Turnaround time
10 workdays
48.4
40
DNA test for the VWF c.1657T>G variant causing autosomal recessive Von Willebrand disease type 2-2 / vWD II in dogs.
Overview
This genetic test examines the VWF variant c.1657T>G in dogs. The variant causes Von Willebrand disease type 2-2 / vWD II, also known as vWD, von Willebrand disease, von Willebrand factor deficiency or an inherited bleeding disorder.
Von Willebrand factor is needed for normal platelet adhesion and helps stabilise factor VIII. When this factor is absent, reduced or dysfunctional, blood clotting becomes less efficient. In Von Willebrand disease type 2-2 / vWD II, this concerns a qualitative abnormality of von Willebrand factor with moderate to severe bleeding risk. This can lead to spontaneous bleeding or prolonged bleeding after minor wounds, teething, dental procedures, surgery, birth or trauma.
Possible signs include nosebleeds, bleeding gums, easy bruising, blood in urine or stool, prolonged bleeding and serious blood loss after procedures. For breed-linked variants, it is important to test the correct VWF variant because different breeds can carry different causal mutations.
This trait is inherited as autosomal recessive. A dog with two normal copies is clear for the tested variant. A dog with one copy is a carrier and can pass the variant on. A dog with two copies is genetically affected: this genotype causes Von Willebrand disease type 2-2 / vWD II for the tested variant.
The result labels are TT, TG and GG.
This test provides practical clarity for breeding, purchase, sale and preparation for situations where bleeding risk matters. In inherited clotting disorders, early carrier detection is especially valuable because healthy carriers can silently pass on the variant and two carriers can produce affected puppies.
Included subanalyses
This analysis includes the following subanalysis:
Allele combinations & result interpretations
Below, for each tested locus, you will find the possible allele combinations that may be reported within this analysis, together with a brief explanation of their genetic meaning. The interpretation of possible interactions between different loci is included in the report, but is not shown here in full because that would lead to too many combinations on this page. The final expression may also depend on other genes and their interaction.
Genotype / allele combination: Clear (TT)
The tested VWF variant c.1657T>G was not detected. This dog will not develop the tested Von Willebrand disease type 2-2 / vWD II due to this variant and will not pass it on.
Genotype / allele combination: Carrier (TG)
One copy of the tested VWF variant c.1657T>G was detected. This dog is a carrier: it will not develop the tested autosomal recessive Von Willebrand disease type 2-2 / vWD II from one copy, but can pass the variant to about half of its offspring. Breed carriers only to clear dogs to prevent affected puppies.
Genotype / allele combination: Genetically affected (GG)
Two copies of the tested VWF variant c.1657T>G were detected. This genotype causes the tested Von Willebrand disease type 2-2 / vWD II and gives a clearly increased risk of severe or prolonged bleeding. This dog will pass the variant to all offspring.
Sampling and submission guidelines





References