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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129935182, TTN
+1 more
(T32799M +5 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GConflicting classifications of pathogenicity
LOC129935182, TTN
+1 more
(N35348K +5 more)
Single nucleotide variant
(missense variant)
Dilated cardiomyopathy 1G
+4 more
GConflicting classifications of pathogenicity
LOC129935182, TTN
+1 more
(D32771fs +5 more)
Deletion
(frameshift variant)
not provided
+4 more
GConflicting classifications of pathogenicity
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