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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VWF
(P1266Q)
Single nucleotide variant
(missense variant)
von Willebrand disease type 1
+5 more
GConflicting classifications of pathogenicity
VWF
(N1231S)
Single nucleotide variant
(missense variant)
von Willebrand disease type 3
+4 more
GConflicting classifications of pathogenicity
VWF
(T1034del)
Deletion
(inframe_deletion)
not specified
+2 more
GConflicting classifications of pathogenicity
VWF
(R854Q)
Single nucleotide variant
(missense variant)
VWF-related condition
+8 more
GPathogenic/Likely pathogenic
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