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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYBPC3
(N1257K)
Single nucleotide variant
(missense variant)
Primary familial dilated cardiomyopathy
+4 more
GConflicting classifications of pathogenicity
MYBPC3
(V219L)
Single nucleotide variant
(missense variant)
Primary familial hypertrophic cardiomyopathy
+6 more
GPathogenic/Likely pathogenic