| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | KYNU, LOC126806361
+1 more | Deletion | Catel-Manzke syndrome | |
| | | Single nucleotide variant (missense variant) | Catel-Manzke syndrome | |
| | | Single nucleotide variant (missense variant) | Catel-Manzke syndrome | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | GPathogenic/Likely pathogenic |
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