| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | SCN1A-AS1, SCN9A (A1627T +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Generalized epilepsy with febrile seizures plus, type 7 +2 more | |
| | SCN1A-AS1, SCN9A (W1168* +1 more) | Single nucleotide variant (nonsense) | Channelopathy-associated congenital insensitivity to pain, autosomal recessive | |
| | SCN9A, SCN1A-AS1 (R907Q +1 more) | Single nucleotide variant (non-coding transcript variant +1 more) | Neuropathy, hereditary sensory and autonomic, type 2A +2 more | GPathogenic/Likely pathogenic |
| | SCN1A-AS1, SCN9A (I720K +1 more) | Single nucleotide variant (missense variant) | not provided +8 more | GConflicting classifications of pathogenicity |
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