| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Autosomal dominant nocturnal frontal lobe epilepsy +1 more | |
| | CHRNA4, LOC126863087 (T109I) | Single nucleotide variant (missense variant +2 more) | Autosomal dominant nocturnal frontal lobe epilepsy +1 more | |
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