| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | Intellectual disability, autosomal recessive 42 | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (nonsense +1 more) | Intellectual disability, autosomal recessive 42 | |
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