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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CTNNA3
(L766del)
Microsatellite
(inframe_deletion)
Arrhythmogenic right ventricular cardiomyopathy
+1 more
GPathogenic
CTNNA3
(V94D +1 more)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 13
GPathogenic