VWF Chromosome 12

Von Willebrand factor
429 variants 429 Health Risk

Upload your DNA to see your personal genotypes for variants in VWF.

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
RS1591874316 Health Risk Likely pathogenic Hereditary von Willebrand disease, Hereditary von Willebrand disease
RS1591886521 Health Risk Likely pathogenic von Willebrand disease type 1, von Willebrand disease type 1
RS1591890769 Health Risk Likely pathogenic Hereditary von Willebrand disease, von Willebrand disease type 2, Hereditary von Willebrand disease
RS1591895308 Health Risk Likely pathogenic Hereditary von Willebrand disease, VWF-related disorder, Hereditary von Willebrand disease
RS1591895879 Health Risk Likely pathogenic Hereditary von Willebrand disease, Hereditary von Willebrand disease
RS1591914708 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS1591924208 Health Risk Likely pathogenic Hereditary von Willebrand disease, Hereditary von Willebrand disease
RS1943194455 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS1943442849 Health Risk Likely pathogenic von Willebrand disease type 1, von Willebrand disease type 1
RS1943611659 Health Risk Likely pathogenic Thrombocytopenia, Thrombocytopenia
RS1944059755 Health Risk Likely pathogenic von Willebrand disease type 1, von Willebrand disease type 1
RS1944671082 Health Risk Likely pathogenic Hereditary von Willebrand disease, Hereditary von Willebrand disease
RS1945427535 Health Risk Likely pathogenic
RS2136338728 Health Risk Likely pathogenic Hereditary von Willebrand disease, Hereditary von Willebrand disease
RS2136339259 Health Risk Likely pathogenic
RS2136376158 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS2136385288 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 1, von Willebrand disease type 3
RS2136385937 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS2136409487 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 2, von Willebrand disease type 3
RS2136409514 Health Risk Likely pathogenic Hereditary von Willebrand disease, von Willebrand disease type 1, Hereditary von Willebrand disease
RS2136411706 Health Risk Likely pathogenic von Willebrand disease type 1, von Willebrand disease type 1
RS2136412168 Health Risk Likely pathogenic von Willebrand disease type 2, von Willebrand disease type 2
RS2136412203 Health Risk Likely pathogenic von Willebrand disease type 2, Von Willebrand disease type 2A, von Willebrand disease type 2
RS2136412350 Health Risk Likely pathogenic von Willebrand disease type 2, von Willebrand disease type 2
RS2136412494 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS2136412581 Health Risk Likely pathogenic von Willebrand disease type 1, von Willebrand disease type 1
RS2136412846 Health Risk Likely pathogenic von Willebrand disease type 2, von Willebrand disease type 2
RS2136413535 Health Risk Likely pathogenic von Willebrand disease type 2, von Willebrand disease type 2
RS2136413547 Health Risk Likely pathogenic Hereditary von Willebrand disease, Von Willebrand disease type 2B, Hereditary von Willebrand disease
RS2136413792 Health Risk Likely pathogenic von Willebrand disease type 1, von Willebrand disease type 1
RS2136413939 Health Risk Likely pathogenic
RS2136418339 Health Risk Likely pathogenic von Willebrand disease type 1, von Willebrand disease type 1
RS2136440319 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS2136454053 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS2136455744 Health Risk Likely pathogenic von Willebrand disease type 2, von Willebrand disease type 2
RS2136470584 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS2136472072 Health Risk Likely pathogenic von Willebrand disease type 1, von Willebrand disease type 1
RS2136500386 Health Risk Likely pathogenic von Willebrand disease type 3, von Willebrand disease type 3
RS2497227296 Health Risk Likely pathogenic
RS2497227407 Health Risk Likely pathogenic Hereditary von Willebrand disease, Hereditary von Willebrand disease
RS2497227417 Health Risk Likely pathogenic
RS2497235136 Health Risk Likely pathogenic Hereditary von Willebrand disease, Hereditary von Willebrand disease
RS2497272240 Health Risk Likely pathogenic Von Willebrand disease type 2B, Von Willebrand disease type 2B
RS2497300203 Health Risk Likely pathogenic VWF-related disorder, VWF-related disorder
RS2497345499 Health Risk Likely pathogenic
RS2497351730 Health Risk Likely pathogenic
RS2497390162 Health Risk Likely pathogenic VWF-related disorder, VWF-related disorder
RS2497390193 Health Risk Likely pathogenic von Willebrand disease type 1, von Willebrand disease type 1
RS2497421036 Health Risk Likely pathogenic
RS2497421495 Health Risk Likely pathogenic von Willebrand disease type 1, von Willebrand disease type 1
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