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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
TTN
(K12841fs)
Deletion
(frameshift variant +1 more)
Hypertrophic cardiomyopathy 9
GUncertain significance
TTN
(E10206Q +2 more)
Single nucleotide variant
(missense variant +1 more)
Dilated cardiomyopathy 1G
+7 more
GUncertain significance
TTN
(K5554* +2 more)
Single nucleotide variant
(nonsense +1 more)
Hypertrophic cardiomyopathy 9
GLikely pathogenic
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