| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (nonsense) | SPATA7-Related Disorders +3 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | SPATA7-Related Disorders +3 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene