| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder +1 more | |
| | | Single nucleotide variant (nonsense) | Intellectual disability, autosomal dominant 6 +2 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder | |
| | | Duplication (frameshift variant) | not provided +2 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene