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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VWF
(R1399C)
Single nucleotide variant
(missense variant)
Hereditary von Willebrand disease
+2 more
GConflicting classifications of pathogenicity
VWF
(R1379C)
Single nucleotide variant
(missense variant)
von Willebrand disease type 1
+4 more
GPathogenic/Likely pathogenic
VWF
(P1266L)
Single nucleotide variant
(missense variant)
VWF-related disorder
+5 more
GConflicting classifications of pathogenicity
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