| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC110121288, SCN10A (I1158M +2 more) | Single nucleotide variant (missense variant) | Brugada syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (splice acceptor variant) | not provided | |
| | LOC110121288, SCN10A (S1059A +2 more) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | LOC110121288, SCN10A (P980L +1 more) | Single nucleotide variant (missense variant) | Brugada syndrome +2 more | |
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