| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (splice donor variant) | SSX1-related disorder | |
| | | Single nucleotide variant (missense variant) | Spermatogenic failure, X-linked, 5 | |
| | | Deletion (frameshift variant) | Spermatogenic failure, X-linked, 5 | |
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