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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT2
(R146H +3 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 2
+2 more
GUncertain significance
TNNT2
(R141W +3 more)
Single nucleotide variant
(missense variant)
Familial isolated dilated cardiomyopathy
+8 more
GPathogenic
TNNT2
(E29fs +2 more)
Deletion
(frameshift variant)
Dilated cardiomyopathy 1D
GUncertain significance
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