| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (non-coding transcript variant +3 more) | Feingold syndrome type 1 | |
| | | Deletion (frameshift variant +2 more) | Feingold syndrome type 1 | |
| | | Single nucleotide variant (missense variant +1 more) | Feingold syndrome type 1 | |
Click to view in NCBI Gene