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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSC2, DSCAS
(G12R)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+6 more
GBenign/Likely benign
DSC2, DSCAS
(N11S)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GBenign
DSC2, DSCAS
(G8V)
Single nucleotide variant
(missense variant)
Familial isolated arrhythmogenic right ventricular dysplasia
+5 more
GConflicting classifications of pathogenicity
DSC2, DSCAS
(S7F)
Single nucleotide variant
(missense variant)
Arrhythmogenic right ventricular dysplasia 11
+2 more
GUncertain significance
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