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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACTN2
(T412M +1 more)
Single nucleotide variant
(missense variant)
Cardiovascular phenotype
+5 more
GConflicting classifications of pathogenicity
ACTN2
(A887T +1 more)
Single nucleotide variant
(missense variant)
ACTN2-related condition
+4 more
GConflicting classifications of pathogenicity