| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | PDE11A, PDE11A-AS1 (T427I +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PDE11A-AS1, PDE11A (T334M +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PDE11A-AS1, PDE11A (C451R +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | PDE11A-AS1, PDE11A (V341A +3 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
Click to view in NCBI Gene