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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSC2
(A897fs)
Duplication
(3 prime UTR variant +1 more)
Cardiovascular phenotype
+6 more
GBenign/Likely benign
DSC2
Single nucleotide variant
(3 prime UTR variant +1 more)
Familial isolated arrhythmogenic right ventricular dysplasia
+4 more
GBenign/Likely benign
DSC2
(G779R)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
DSC2
(Q638H)
Single nucleotide variant
(missense variant)
DSC2-related condition
+6 more
GConflicting classifications of pathogenicity
DSC2
(F58V)
Single nucleotide variant
(missense variant)
Familial isolated arrhythmogenic right ventricular dysplasia
+6 more
GConflicting classifications of pathogenicity
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