| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | SCN9A, SCN1A-AS1 (L1612P +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided | |
| | SCN9A, SCN1A-AS1 (F1462V +1 more) | Single nucleotide variant (missense variant) | Paroxysmal extreme pain disorder | |
| | SCN1A-AS1, SCN9A (I1461N +1 more) | Single nucleotide variant (missense variant) | Generalized epilepsy with febrile seizures plus, type 7 +1 more | |
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