| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (synonymous variant) | Primary erythromelalgia +4 more | |
| | SCN9A, SCN1A-AS1 (N1245S +1 more) | Single nucleotide variant (missense variant) | Paroxysmal extreme pain disorder +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +7 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene