| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC130064822, LOC130064823
+290 more | Copy number gain | See cases | |
| | LOC130064925, LOC130064926
+1081 more | Copy number gain | See cases | |
| | LOC130064903, LOC130064904
+1093 more | Copy number gain | See cases | |
| | GRIN2D, LOC130064856 (S134*) | Single nucleotide variant (nonsense) | not provided | |
| | GRIN2D, LOC130064856 (P154A) | Single nucleotide variant (missense variant) | not provided | |
Click to view in NCBI Gene