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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSC2
(M589T)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
DSC2
Single nucleotide variant
(synonymous variant)
not provided
+5 more
GBenign/Likely benign
DSC2
Single nucleotide variant
(synonymous variant)
not specified
+1 more
GLikely benign
DSC2
Single nucleotide variant
(intron variant)
Cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
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