| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (5 prime UTR variant) | STK38L-related disorder | |
| | | Single nucleotide variant (synonymous variant) | STK38L-related disorder +1 more | |
| | | Duplication (intron variant) | STK38L-related disorder | |
| | | Deletion (intron variant) | STK38L-related disorder | |
Click to view in NCBI Gene