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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNC1
(D25N)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+3 more
GUncertain significance
TNNC1
(A8V)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GPathogenic/Likely pathogenic