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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYBPC3
(R502W)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+7 more
GPathogenic/Likely pathogenic
MYBPC3
(R495Q)
Single nucleotide variant
(missense variant)
Left ventricular noncompaction 10
+8 more
GPathogenic/Likely pathogenic
MYBPC3
(K368*)
Single nucleotide variant
(nonsense)
Hypertrophic cardiomyopathy 4
+1 more
GLikely pathogenic
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