| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | GRIK4, LOC101929208 (E572K) | Single nucleotide variant (missense variant) | not provided | |
| | LOC101929208, GRIK4 (S622N) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC101929208, GRIK4 (L552F) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | GRIK4, LOC101929208 (R619H) | Single nucleotide variant (missense variant) | not provided | |
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