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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VWF
(V1934G)
Single nucleotide variant
(missense variant)
Thrombocytopenia
+2 more
GConflicting classifications of pathogenicity
VWF
(G1631D)
Single nucleotide variant
(missense variant)
von Willebrand disease type 2
+1 more
GPathogenic/Likely pathogenic