| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Kostmann syndrome | |
| | | Duplication (frameshift variant) | Inborn genetic diseases +1 more | |
| | | Duplication (frameshift variant) | not provided +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Kostmann syndrome | |
Click to view in NCBI Gene