| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | MXD3, PRELID1 (A193V +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | MXD3, PRELID1 (Q212K +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | MXD3, PRELID1 (Q206H +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | MXD3, PRELID1 (F207C +1 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
Click to view in NCBI Gene