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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TNNT2
Single nucleotide variant
(synonymous variant)
TNNT2-related condition
+7 more
GConflicting classifications of pathogenicity
TNNT2
(R141W +3 more)
Single nucleotide variant
(missense variant)
Familial isolated dilated cardiomyopathy
+8 more
GPathogenic
TNNT2
Microsatellite
(intron variant)
Dilated Cardiomyopathy, Dominant
+9 more
GBenign/Likely benign
TNNT2
Single nucleotide variant
(intron variant)
TNNT2-related condition
+5 more
GConflicting classifications of pathogenicity
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