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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806433, TTN
Single nucleotide variant
(intron variant)
Primary dilated cardiomyopathy
GUncertain significance
LOC126806433, TTN
Duplication
(splice donor variant)
not provided
+1 more
GConflicting classifications of pathogenicity