| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Duplication (inframe_insertion +2 more) | Autosomal dominant nocturnal frontal lobe epilepsy +3 more | GConflicting classifications of pathogenicity |
| | CHRNA4, LOC100130587 (P6A) | Single nucleotide variant (non-coding transcript variant +2 more) | not provided | |
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