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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CASQ1
(G383fs)
Deletion
(frameshift variant)
not provided
+1 more
GUncertain significance
ETFDH
(Y243C +2 more)
Single nucleotide variant
(missense variant)
Myopathy
GUncertain significance
ETFDH
(D456V +2 more)
Single nucleotide variant
(missense variant)
Myopathy
GUncertain significance
FBN1
(D2607N)
Single nucleotide variant
(missense variant)
Myopathy
+2 more
GLikely pathogenic
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