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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MYH2, MYHAS
(R1838fs)
Duplication
(frameshift variant)
Myopathy
GLikely pathogenic
MYH2, MYHAS
(T1257fs)
Deletion
(frameshift variant)
Myopathy
GLikely pathogenic