| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | CDK13, LOC129998292 (A162fs) | Duplication (frameshift variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene