| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Indel (missense variant +1 more) | Generalized hypotonia +6 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 8 +6 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene