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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSG2
(F388C)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GUncertain significance
DSG2, DSG2-AS1
(I851fs)
Deletion
(frameshift variant)
Arrhythmogenic right ventricular dysplasia 10
+1 more
GPathogenic/Likely pathogenic
DSG2, DSG2-AS1
(E1018fs)
Duplication
(frameshift variant)
Cardiovascular phenotype
+2 more
GConflicting classifications of pathogenicity
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