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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT2
(R278C +5 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 2
+9 more
GConflicting classifications of pathogenicity
TNNT2
(E116fs +2 more)
Deletion
(frameshift variant +1 more)
Dilated cardiomyopathy 1D
+5 more
GConflicting classifications of pathogenicity