| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (nonsense) | Neurodevelopmental disorder with ataxia, hypotonia, and microcephaly +4 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +12 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene