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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VWF
(P1684R)
Single nucleotide variant
(missense variant)
von Willebrand disease type 1
GUncertain significance
VWF
(P1266Q)
Single nucleotide variant
(missense variant)
von Willebrand disease type 1
+5 more
GConflicting classifications of pathogenicity