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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT2
(W287* +5 more)
Single nucleotide variant
(nonsense)
Hypertrophic cardiomyopathy
+7 more
GPathogenic/Likely pathogenic
TNNT2
(R141W +3 more)
Single nucleotide variant
(missense variant)
Familial isolated dilated cardiomyopathy
+8 more
GPathogenic