| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | CHRNA4, LOC126863087 (P121L) | Single nucleotide variant (missense variant +2 more) | Autosomal dominant nocturnal frontal lobe epilepsy +2 more | |
| | | Single nucleotide variant (synonymous variant +2 more) | CHRNA4-related disorder +1 more | |
| | CHRNA4, LOC126863087 (E92Q) | Single nucleotide variant (missense variant +2 more) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Autosomal dominant nocturnal frontal lobe epilepsy +1 more | |
| | CHRNA4, LOC126863087 (N80K) | Single nucleotide variant (missense variant +2 more) | CHRNA4-related disorder | |
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