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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
DES
(S28F)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
GUncertain significance
DES
(G65S)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1I
+5 more
GConflicting classifications of pathogenicity