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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MTM1
(A34fs)
Deletion
(frameshift variant)
Severe X-linked myotubular myopathy
GLikely pathogenic
MTM1
(V49I)
Single nucleotide variant
(missense variant)
Severe X-linked myotubular myopathy
GConflicting classifications of pathogenicity
MTM1
Single nucleotide variant
(splice acceptor variant)
Severe X-linked myotubular myopathy
GLikely pathogenic
MTM1
(D220G +1 more)
Single nucleotide variant
(missense variant)
Severe X-linked myotubular myopathy
GUncertain significance
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