| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | SCN1A-AS1, SCN9A (E1841A +1 more) | Single nucleotide variant (missense variant) | Neuropathy, hereditary sensory and autonomic, type 2A +3 more | |
| | SCN9A, SCN1A-AS1 (D1690G +1 more) | Single nucleotide variant (missense variant) | Channelopathy-associated congenital insensitivity to pain, autosomal recessive | |
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