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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACTN2
(A732T +1 more)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1AA
+6 more
GConflicting classifications of pathogenicity
ACTN2
(D633fs +1 more)
Deletion
(frameshift variant)
Myopathy, distal, 6, adult-onset, autosomal dominant
+1 more
GConflicting classifications of pathogenicity