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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VWF
(R2507G)
Single nucleotide variant
(missense variant)
von Willebrand disease type 1
GUncertain significance
VWF
(Q1311*)
Single nucleotide variant
(nonsense)
Hereditary von Willebrand disease
+2 more
GPathogenic