| | | Single nucleotide variant (3 prime UTR variant) | Intellectual Disability, Dominant +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided | |
| | | Single nucleotide variant (3 prime UTR variant) | Intellectual Disability, Dominant | |
| | | Single nucleotide variant (3 prime UTR variant) | Intellectual Disability, Dominant | |
| | | Deletion (3 prime UTR variant) | Intellectual Disability, Dominant | |
| | | Deletion (3 prime UTR variant) | Intellectual Disability, Dominant | |
| | | Deletion (frameshift variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Developmental and epileptic encephalopathy, 27 +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Deletion (inframe_deletion +1 more) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +2 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +2 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Landau-Kleffner syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +4 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Indel (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Duplication (frameshift variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | GRIN2B-related disorder | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Inborn genetic diseases +2 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +2 more | |
| | | Single nucleotide variant (missense variant) | GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +2 more | |
| | | Deletion (nonsense) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +2 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Microsatellite (inframe_deletion) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +3 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Developmental and epileptic encephalopathy, 27 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | Intellectual disability, autosomal dominant 6 +4 more | |
| | | Single nucleotide variant (missense variant) | Intellectual disability, autosomal dominant 6 +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |