| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Microcephaly, normal intelligence and immunodeficiency +4 more | |
| | | Single nucleotide variant (splice donor variant) | Microcephaly, normal intelligence and immunodeficiency +3 more | GConflicting classifications of pathogenicity |
| | LOC126860438, NBN (R624H +1 more) | Single nucleotide variant (missense variant) | Aplastic anemia +3 more | |
| | | Deletion (frameshift variant) | Aplastic anemia +3 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Deletion (frameshift variant) | Microcephaly, normal intelligence and immunodeficiency +7 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly, normal intelligence and immunodeficiency +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Hereditary cancer-predisposing syndrome +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Aplastic anemia +4 more | |
| | | Single nucleotide variant (missense variant) | Microcephaly, normal intelligence and immunodeficiency +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hereditary cancer-predisposing syndrome +4 more | |
Click to view in NCBI Gene