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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
ACTA1
(D246E)
Single nucleotide variant
(missense variant)
Actin accumulation myopathy
+1 more
GConflicting classifications of pathogenicity
ACTA1
(E228*)
Single nucleotide variant
(nonsense)
Congenital myopathy with fiber type disproportion
+1 more
GPathogenic
ACTA1
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
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