RS41276738 VWF
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What This Variant Does
"rs41276738, also known as c.2561G>
Associated Conditions
von Willebrand disease type 2N
von Willebrand disease type 1
Hereditary von Willebrand disease
von Willebrand disease type 2
von Willebrand disease type 3
Abnormality of coagulation
Thrombocytopenia
Abnormal bleeding
VWF-related disorder
von Willebrand disorder
von Willebrand disease type 2N
von Willebrand disease type 1
Hereditary von Willebrand disease
von Willebrand disease type 2
von Willebrand disease type 3
Other Variants in VWF