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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH7
(A1379T)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy 1
+5 more
GPathogenic/Likely pathogenic
MYH7
(R904C)
Single nucleotide variant
(missense variant)
Primary dilated cardiomyopathy
GPathogenic
MYH7
(R143Q)
Single nucleotide variant
(missense variant)
Hypertrophic cardiomyopathy
GLikely pathogenic
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