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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ADAMTS13
(R421C +1 more)
Single nucleotide variant
(missense variant)
not provided
+2 more
GConflicting classifications of pathogenicity
ADAMTS13
(T1135M)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GConflicting classifications of pathogenicity
ADAMTS13
(H1109Q +2 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
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