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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSG2, LOC130062340
Single nucleotide variant
(5 prime UTR variant)
Arrhythmogenic right ventricular dysplasia 10
+1 more
GUncertain significance
DSG2, LOC130062340
Single nucleotide variant
(intron variant)
Cardiovascular phenotype
+3 more
GUncertain significance
DSG2, LOC130062340
Single nucleotide variant
(intron variant)
Arrhythmogenic right ventricular dysplasia 10
+2 more
GBenign/Likely benign
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