RS1800386 VWF

Health Risk Chr 12:6018667
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What This Variant Does
"rs1800386, also known as c.4751A&gt
Associated Conditions
Hereditary von Willebrand disease
Inborn genetic diseases
von Willebrand disease type 2
von Willebrand disease type 1
Thrombus
Thrombocytopenia
VWF-related disorder
von Willebrand disorder
von Willebrand disease type 3
Hereditary von Willebrand disease
Inborn genetic diseases
von Willebrand disease type 2
von Willebrand disease type 1
Thrombus
Thrombocytopenia
Other Variants in VWF
rs61750584 rs61750117 rs61750579 rs61749392 rs61749384 rs61749387 rs61749397 rs61749403 rs61748477 rs121964894
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