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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS13
(N614T +1 more)
Single nucleotide variant
(missense variant +1 more)
Upshaw-Schulman syndrome
+2 more
GUncertain significance
ADAMTS13
(V770M +1 more)
Single nucleotide variant
(missense variant)
Upshaw-Schulman syndrome
+1 more
GConflicting classifications of pathogenicity