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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC126806433, TTN
(R2354C +1 more)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
+6 more
GConflicting classifications of pathogenicity
LOC126806433, TTN
(E2259D +1 more)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GLikely benign