| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | GRIN2C, LOC130061625 (R183H) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | GRIN2C, LOC130061625 (V182G) | Single nucleotide variant (missense variant +1 more) | not specified | |
| | GRIN2C, LOC130061625 (V182A) | Single nucleotide variant (missense variant +1 more) | not specified | |
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