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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DSG2, LOC130062340
Deletion
(5 prime UTR variant)
Cardiomyopathy
GUncertain significance
DSG2, LOC130062340
Single nucleotide variant
(synonymous variant)
Cardiomyopathy
+6 more
GBenign/Likely benign
DSG2, LOC130062340
(L15Q)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
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