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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYBPC3
(R980C)
Single nucleotide variant
(missense variant)
Cardiomyopathy
+7 more
GConflicting classifications of pathogenicity
MYBPC3
(A833T)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+7 more
GConflicting classifications of pathogenicity
MIB1
(I248V)
Single nucleotide variant
(missense variant)
Paroxysmal atrial fibrillation
GUncertain significance
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