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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
VCL
(L277M)
Single nucleotide variant
(missense variant)
Primary familial dilated cardiomyopathy
+7 more
GConflicting classifications of pathogenicity
VCL
(L955del)
Deletion
(inframe_deletion +1 more)
Primary dilated cardiomyopathy
+5 more
GConflicting classifications of pathogenicity
VCL
(R975W)
Single nucleotide variant
(missense variant +1 more)
Cardiovascular phenotype
+2 more
GUncertain significance
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