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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS13
(E778K +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
ADAMTS13
(R1060W +1 more)
Single nucleotide variant
(missense variant +1 more)
ADAMTS13-related condition
+3 more
GPathogenic/Likely pathogenic