| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | GNL2, LOC126805705 (K415E +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GNL2, LOC126805705 (E578K +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | GNL2, LOC126805705 (V494I +2 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene