| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy | |
| | LOC126862278, RBFOX1 (T118M +2 more) | Single nucleotide variant (missense variant) | Idiopathic generalized epilepsy | |
| | LOC126862279, RBFOX1 (A366T +3 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
Click to view in NCBI Gene