Gene entry
VWF
von Willebrand factor
- Chromosome
- 12
- Cytoband
- 12p13.31
- Variants (rsID)
- 78
VWF is a protein-coding gene, meaning the body reads it as instructions to build a protein, located on chromosome 12 (region 12p13.31). Its official name is “von Willebrand factor”. The reference table lists 78 variants (rsID) for this gene.
Clinically classified variants
29 reference-table entries with clinical significance.
- rs11063962Benignsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 2|von Willebrand disease type 3|von Willebrand disease type 1
- rs11063987Benignsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 2|von Willebrand disease type 1|von Willebrand disease type 3
- rs141087261Benignsingle nucleotide variantvon Willebrand disease type 3|von Willebrand disease type 2|von Willebrand disease type 1
- rs1800377Benignsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 1|von Willebrand disease type 2|von Willebrand disease type 3
- rs1800378Benignsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 3|von Willebrand disease type 2|von Willebrand disease type 1
- rs1800379Benignsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 1|von Willebrand disease type 2|von Willebrand disease type 3
- rs216321Benignsingle nucleotide variant
- rs216902Benignsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 2|von Willebrand disease type 1|von Willebrand disease type 3
- rs57950734Benignsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 2|von Willebrand disease type 1|von Willebrand disease type 3
- rs61750615Benignsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 1|von Willebrand disease type 2|von Willebrand disease type 3
- rs78302129Benignsingle nucleotide variant
- rs7962217Benignsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 2|von Willebrand disease type 1|von Willebrand disease type 3
- rs7980045Benignsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 1|von Willebrand disease type 3|von Willebrand disease type 2
- rs1800386Conflicting interpretationssingle nucleotide variantvon Willebrand disease, type 1, susceptibility to|Inborn genetic diseases|von Willebrand disorder|von Willebrand disease type 2|von Willebrand disease type 1|Thrombus
- rs33978901Conflicting interpretationssingle nucleotide variantvon Willebrand disease type 3|von Willebrand disease type 2|von Willebrand disease type 1
- rs34230288Conflicting interpretationssingle nucleotide variant
- rs55687637Conflicting interpretationssingle nucleotide variantvon Willebrand disorder
- rs76505074Conflicting interpretationssingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 1
- rs121964894Pathogenicsingle nucleotide variantvon Willebrand disease type 2N|von Willebrand disorder
- rs41276738Pathogenicsingle nucleotide variantvon Willebrand disease type 2N|von Willebrand disease type 1|von Willebrand disorder|von Willebrand disease type 2|von Willebrand disease type 2|von Willebrand disease type 3|von Willebrand disease type 1|Abnormality of coagulation|Thrombocytopenia|Abnormal bleeding
- rs61748467Pathogenicsingle nucleotide variantvon Willebrand disease type 1
- rs61749397Pathogenicsingle nucleotide variantVon Willebrand disease type 2B|von Willebrand disorder|von Willebrand disease type 2
- rs61749398Pathogenicsingle nucleotide variantvon Willebrand disease type 2M
- rs61750074Pathogenicsingle nucleotide variantvon Willebrand disorder|von Willebrand disease type 2|von Willebrand disease type 1
- rs61751286Pathogenicsingle nucleotide variantvon Willebrand disorder|Thrombocytopenia|Abnormal bleeding|von Willebrand disease type 1
- rs61751296Pathogenicsingle nucleotide variantvon Willebrand disease type 3|von Willebrand disorder|von Willebrand disease type 1
- rs61754010Pathogenicsingle nucleotide variantVon Willebrand disease type 2A|von Willebrand disease type 2
- rs61753991Uncertain significancesingle nucleotide variant
- rs62643631Uncertain significancesingle nucleotide variantAbnormal bleeding
Other listed variants
- rs216294
- rs216334
- rs216811
- rs216855
- rs216865
- rs216873
- rs216880
- rs917859
- rs980131
- rs2238106
- rs2239158
- rs2283332
- rs2286608
- rs2286646
- rs3819537
- rs4764534
- rs7135976
- rs11063961
- rs11064024
- rs11837584
- rs12317523
- rs12319392
- rs36007563
- rs56311842
- rs60982029
- rs71582859
- rs71582860
- rs71582882
- rs73034900
- rs75649740
- rs76484124
- rs77344012
- rs78158784
Public references
Data from the institutional reference table and public NCBI annotation. For education only; not a substitute for medical or genetic counselling.