| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126862279, RBFOX1 (T351M +1 more) | Single nucleotide variant (synonymous variant +1 more) | Idiopathic generalized epilepsy +1 more | |
| | LOC126862279, RBFOX1 (L366F +15 more) | Single nucleotide variant (missense variant +1 more) | Inborn genetic diseases | |
| | LOC126862279, RBFOX1 (P348A +3 more) | Single nucleotide variant (missense variant +1 more) | Idiopathic generalized epilepsy +1 more | |
| | LOC126862279, RBFOX1 (P374S +30 more) | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | LOC126862279, RBFOX1 (A371V +1 more) | Single nucleotide variant (synonymous variant +1 more) | Idiopathic generalized epilepsy +1 more | |
Click to view in NCBI Gene