| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant +1 more) | Myopathy, reducing body, X-linked, childhood-onset +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | X-linked myopathy with postural muscle atrophy +1 more | |
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