| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | von Willebrand disease type 1 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | von Willebrand disease type 1 | |
| | | Single nucleotide variant (missense variant) | Hereditary von Willebrand disease +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | von Willebrand disease type 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary von Willebrand disease +8 more | GConflicting classifications of pathogenicity; risk factor |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | von Willebrand disease type 2 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | von Willebrand disease type 2 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Deletion (inframe_deletion) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | von Willebrand disease type 2N | |
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