| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity; risk factor |
| | | Single nucleotide variant (missense variant) | Hereditary von Willebrand disease +8 more | GPathogenic/Likely pathogenic |
| | | Indel (missense variant) | not specified +2 more | |
| | | Single nucleotide variant (missense variant) | von Willebrand disease type 1 +1 more | |
Click to view in NCBI Gene