| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126860438, NBN (K635* +1 more) | Single nucleotide variant (nonsense) | Aplastic anemia +4 more | GPathogenic/Likely pathogenic |
| | LOC126860438, NBN (E628K +1 more) | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +6 more | |
Click to view in NCBI Gene