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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
PKP2
(V200M)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular cardiomyopathy
+3 more
GUncertain significance
PKP2
(L32M)
Single nucleotide variant
(missense variant +1 more)
Arrhythmogenic right ventricular dysplasia 9
GUncertain significance
PKP2
Deletion
Arrhythmogenic right ventricular dysplasia 9
GPathogenic
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