RS61748477 VWF
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What This Variant Does
"rs61748477, also known as c.2372C>
Associated Conditions
von Willebrand disease type 2N
Abnormal bleeding
Hereditary von Willebrand disease
von Willebrand disease type 2
von Willebrand disease type 2N
Abnormal bleeding
Hereditary von Willebrand disease
von Willebrand disease type 2
Other Variants in VWF