RS61750117 VWF
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What This Variant Does
"rs61750117, also known as c.4789C>
Associated Conditions
Von Willebrand disease type 2A
Inborn genetic diseases
Hereditary von Willebrand disease
von Willebrand disease type 2
Von Willebrand disease type 2A
Inborn genetic diseases
Hereditary von Willebrand disease
von Willebrand disease type 2
Other Variants in VWF