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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT2
(K210del +5 more)
Microsatellite
(inframe_deletion)
Cardiovascular phenotype
+6 more
GPathogenic/Likely pathogenic
TNNT2
(R173Q +3 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
+5 more
GPathogenic/Likely pathogenic