| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC125078019, NRDE2 (G442E) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC125078019, NRDE2 (N377S) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene