RS61749384 VWF
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What This Variant Does
"rs61749384, also known as c.3916C>
Associated Conditions
Von Willebrand disease type 2B
Hereditary von Willebrand disease
von Willebrand disease type 2
Abnormality of coagulation
von Willebrand disease type 1
von Willebrand disease type 3
von Willebrand disorder
Von Willebrand disease type 2B
Hereditary von Willebrand disease
von Willebrand disease type 2
Abnormality of coagulation
von Willebrand disease type 1
von Willebrand disease type 3
von Willebrand disorder
Other Variants in VWF