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Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSG2, DSG2-AS1
(E713K)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GBenign/Likely benign
DSG2, DSG2-AS1
(V920G)
Single nucleotide variant
(missense variant)
DSG2-related condition
+6 more
GBenign/Likely benign
DSG2, DSG2-AS1
(T1070M)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GBenign/Likely benign
DSG2, DSG2-AS1
(P1082A)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
DSG2, DSG2-AS1
Single nucleotide variant
(3 prime UTR variant)
Cardiovascular phenotype
+4 more
GConflicting classifications of pathogenicity
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