| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (no sequence alteration +1 more) | Brugada syndrome +5 more | |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome +4 more | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | |
| | LOC110121288, SCN10A (L1092P +2 more) | Single nucleotide variant (missense variant) | not specified +4 more | |
| | SCN10A, LOC110121288 (V1073A +2 more) | Single nucleotide variant (missense variant) | Brugada syndrome +4 more | |
| | | Single nucleotide variant (synonymous variant) | Brugada syndrome +4 more | |
| | LOC110121288, SCN10A (I962V +1 more) | Single nucleotide variant (missense variant) | Brugada syndrome +4 more | |
| | | Single nucleotide variant (intron variant) | Brugada syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not specified +4 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +4 more | |
| | | Single nucleotide variant (intron variant) | not provided +3 more | |
Click to view in NCBI Gene