VWF Chromosome 12

Von Willebrand factor
429 variants 429 Health Risk

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What This Gene Does
This gene encodes a glycoprotein involved in hemostasis. The encoded preproprotein is proteolytically processed following assembly into large multimeric complexes. These complexes function in the adhesion of platelets to sites of vascular injury and the transport of various proteins in the blood. Mutations in this gene result in von Willebrand disease, an inherited bleeding disorder. An unprocessed pseudogene has been found on chromosome 22. [provided by RefSeq, Oct 2015]
Gene Info
Gene Group
Receptor ligands
Locus Type
gene with protein product
Location
12p13.31
Ensembl
ENSG00000110799
Associated Conditions (38)
VWF-related disorder
von Willebrand disease type 3
von Willebrand disease type 1
Hereditary von Willebrand disease
von Willebrand disorder
Inborn genetic diseases
von Willebrand disease type 2
See cases
Abnormality of coagulation
Nonpapillary renal cell carcinoma
Clear cell carcinoma of kidney
Sarcoma
Uterine corpus endometrial carcinoma
Abnormal bleeding
Thrombocytopenia
Malignant tumor of urinary bladder
Heterotopia
periventricular
X-linked dominant
Colon adenocarcinoma
+18 more conditions
Key Variants
RS112319661
Conflicting classifications of pathogenicity
VWF-related disorder, VWF-related disorder
Health Risk
RS113814258
Conflicting classifications of pathogenicity
von Willebrand disease type 3, von Willebrand disease type 1, Hereditary von Willebrand disease
Health Risk
RS11837584
Conflicting classifications of pathogenicity
von Willebrand disease type 3, von Willebrand disease type 1, von Willebrand disease type 3
Health Risk
RS1223422347
Conflicting classifications of pathogenicity
von Willebrand disease type 3, von Willebrand disorder, von Willebrand disease type 3
Health Risk
RS1229452874
Conflicting classifications of pathogenicity
von Willebrand disorder, VWF-related disorder, von Willebrand disorder
Health Risk
RS1287088175
Conflicting classifications of pathogenicity
Health Risk
RS1312908190
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS139196998
Conflicting classifications of pathogenicity
von Willebrand disease type 2, von Willebrand disease type 1, von Willebrand disease type 3
Health Risk
RS139845585
Conflicting classifications of pathogenicity
Hereditary von Willebrand disease, von Willebrand disease type 1, See cases
Health Risk
RS139864572
Conflicting classifications of pathogenicity
Hereditary von Willebrand disease, Hereditary von Willebrand disease
Health Risk
RS140464171
Conflicting classifications of pathogenicity
Hereditary von Willebrand disease, Inborn genetic diseases, Hereditary von Willebrand disease
Health Risk
RS141649383
Conflicting classifications of pathogenicity
von Willebrand disease type 2, von Willebrand disease type 1, von Willebrand disease type 3
Health Risk
All Variants (429)
RSID Category Clinical Significance Conditions
RS61750071 Health Risk Pathogenic Hereditary von Willebrand disease, von Willebrand disease type 2, von Willebrand disorder
RS61750077 Health Risk Pathogenic Hereditary von Willebrand disease, von Willebrand disease type 2, von Willebrand disorder
RS61750078 Health Risk Pathogenic von Willebrand disease type 2M, von Willebrand disease type 2, Hereditary von Willebrand disease
RS61750089 Health Risk Pathogenic
RS61750094 Health Risk Pathogenic
RS61750095 Health Risk Pathogenic Abnormality of coagulation, Abnormality of coagulation
RS61750103 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS61750112 Health Risk Pathogenic von Willebrand disorder, von Willebrand disorder
RS61750117 Health Risk Pathogenic Von Willebrand disease type 2A, Inborn genetic diseases, Hereditary von Willebrand disease
RS61750577 Health Risk Pathogenic Hereditary von Willebrand disease, von Willebrand disease type 2, Hereditary von Willebrand disease
RS61750580 Health Risk Pathogenic von Willebrand disease type 2, Hereditary von Willebrand disease, Von Willebrand disease type 2A
RS61750584 Health Risk Pathogenic Von Willebrand disease type 2A, Hereditary von Willebrand disease, von Willebrand disease type 2
RS61750585 Health Risk Pathogenic Von Willebrand disease type 2A, von Willebrand disease type 2, Von Willebrand disease type 2A
RS61750595 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 1, Hereditary von Willebrand disease
RS61750602 Health Risk Pathogenic
RS61750606 Health Risk Pathogenic von Willebrand disease type 3, See cases, von Willebrand disease type 2
RS61750612 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 1, Hereditary von Willebrand disease
RS61750614 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS61750617 Health Risk Pathogenic
RS61750623 Health Risk Pathogenic Hereditary von Willebrand disease, Hereditary von Willebrand disease
RS61750630 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS61751296 Health Risk Pathogenic von Willebrand disease type 3, Hereditary von Willebrand disease, von Willebrand disease type 1
RS61751297 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS61751310 Health Risk Pathogenic Von Willebrand disease type 2A, Von Willebrand disease type 2A
RS61751311 Health Risk Pathogenic Von Willebrand disease type 2A, Von Willebrand disease type 2A
RS61753984 Health Risk Pathogenic von Willebrand disease type 2, VWF-related disorder, von Willebrand disease type 3
RS61753988 Health Risk Pathogenic von Willebrand disease type 2, von Willebrand disease type 3, von Willebrand disease type 2
RS61754000 Health Risk Pathogenic von Willebrand disease type 3, Hereditary von Willebrand disease, von Willebrand disease type 1
RS61754002 Health Risk Pathogenic von Willebrand disease type 2N, von Willebrand disease type 2N
RS61754003 Health Risk Pathogenic von Willebrand disease type 3, VWF-related disorder, von Willebrand disease type 3
RS61754004 Health Risk Pathogenic
RS61754005 Health Risk Pathogenic von Willebrand disease type 1, von Willebrand disease type 1
RS61754010 Health Risk Pathogenic Von Willebrand disease type 2A, von Willebrand disease type 2, Von Willebrand disease type 2A
RS61754011 Health Risk Pathogenic Von Willebrand disease type 2A, Von Willebrand disease type 2A
RS62643623 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS62643624 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS62643625 Health Risk Pathogenic Hereditary von Willebrand disease, Hereditary von Willebrand disease
RS62643632 Health Risk Pathogenic von Willebrand disease type 3, Hereditary von Willebrand disease, Abnormal bleeding
RS62643640 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS746648486 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS750364485 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS753701755 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS758895722 Health Risk Pathogenic von Willebrand disease type 1, von Willebrand disorder, VWF-related disorder
RS764755360 Health Risk Pathogenic
RS767837153 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS770203987 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS774210583 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS776747320 Health Risk Pathogenic von Willebrand disease type 3, von Willebrand disease type 3, von Willebrand disease type 3
RS779819811 Health Risk Pathogenic Thrombocytopenia, Thrombocytopenia
RS1055962685 Health Risk Pathogenic/Likely pathogenic
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