| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases +2 more | GConflicting classifications of pathogenicity |
| | LOC126806652, SCN11A (P1176A) | Single nucleotide variant (missense variant) | Hereditary sensory and autonomic neuropathy type 7 +1 more | |
| | | Single nucleotide variant (missense variant) | Familial episodic pain syndrome with predominantly lower limb involvement +2 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | GConflicting classifications of pathogenicity |
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