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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSC2
(I776M)
Single nucleotide variant
(missense variant)
Familial isolated arrhythmogenic right ventricular dysplasia
+3 more
GUncertain significance
DSC2
(G220R)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GUncertain significance
DSC2
(V188M +1 more)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 11
+1 more
GUncertain significance
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