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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH7
(R904C)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GPathogenic
MYH7
(R143Q)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
GLikely pathogenic