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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT2
(R286H +5 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+6 more
GUncertain significance
TNNT2
(E244D +5 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+8 more
GConflicting classifications of pathogenicity
TNNT2
(P77L +3 more)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+6 more
GUncertain significance
TNNT2
(A28V +2 more)
Single nucleotide variant
Supraventricular tachycardia
+8 more
GConflicting classifications of pathogenicity
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