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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS13
(V282E)
Single nucleotide variant
(missense variant +1 more)
Upshaw-Schulman syndrome
GUncertain significance
ADAMTS13
(R421C +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ADAMTS13
(E641K +2 more)
Single nucleotide variant
(missense variant +1 more)
Upshaw-Schulman syndrome
GLikely pathogenic
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