| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Hereditary cancer-predisposing syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Acute lymphoid leukemia +5 more | |
| | LOC126860438, NBN (E628K +1 more) | Single nucleotide variant (missense variant) | Acute lymphoid leukemia +6 more | |
Click to view in NCBI Gene