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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYBPC3
Deletion
MYBPC3-related condition
+6 more
GConflicting classifications of pathogenicity
MYBPC3
(F864fs)
Duplication
(frameshift variant)
Hypertrophic cardiomyopathy
+1 more
GPathogenic/Likely pathogenic
MYBPC3
Single nucleotide variant
(intron variant)
Hypertrophic cardiomyopathy 4
+6 more
GPathogenic/Likely pathogenic
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