| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | GRIA4, LOC126861324 (C153R) | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder with or without seizures and gait abnormalities | |
| | | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Neurodevelopmental disorder with or without seizures and gait abnormalities | |
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