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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSC2
(N573D)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+2 more
GUncertain significance
DSC2
(T268A)
Single nucleotide variant
(missense variant)
not specified
+5 more
GConflicting classifications of pathogenicity
DSC2
Duplication
(intron variant)
Arrhythmogenic right ventricular dysplasia 11
+1 more
GBenign/Likely benign
DSC2
(R203C)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+2 more
GUncertain significance
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