| | LOC110121269, SCN5A (R1115W +1 more) | Single nucleotide variant (missense variant +1 more) | Brugada syndrome 1 +10 more | |
| | LOC110121269, SCN5A (A1112V +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiac arrhythmia +9 more | |
| | LOC110121269, SCN5A (S1102F +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +10 more | |
| | LOC110121269, SCN5A (S1103Y +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +15 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (A1102T +1 more) | Single nucleotide variant (missense variant +1 more) | Brugada syndrome 1 +9 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (A1099V +1 more) | Single nucleotide variant (missense variant +1 more) | Brugada syndrome 1 +10 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (P1089L +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +13 more | |
| | LOC110121269, SCN5A (G1083S +1 more) | Single nucleotide variant (missense variant +1 more) | Brugada syndrome 1 +9 more | |
| | LOC110121269, SCN5A (S1078F +1 more) | Single nucleotide variant (missense variant +1 more) | Brugada syndrome 1 +9 more | |
| | LOC110121269, SCN5A (S1078T +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +10 more | |
| | LOC110121269, SCN5A (E1072S) | Inversion (missense variant) | not provided +10 more | |
| | LOC110121269, SCN5A (A1050T) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +10 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (G1040R) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +10 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (Q1033R) | Single nucleotide variant (missense variant) | Brugada syndrome 1 +9 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +11 more | |
| | LOC110121269, SCN5A (R1027Q) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +11 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (R1027W) | Single nucleotide variant (missense variant) | Brugada syndrome +10 more | |
| | LOC110121269, SCN5A (R1023P) | Single nucleotide variant (missense variant) | Long QT syndrome 3 +10 more | |
| | LOC110121269, SCN5A (A997S) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +10 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (R988Q) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +11 more | |
| | LOC110121269, SCN5A (R988W) | Single nucleotide variant (missense variant) | not provided +9 more | |
| | LOC110121269, SCN5A (R975Q) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +10 more | |
| | LOC110121269, SCN5A (R975W) | Single nucleotide variant (missense variant) | Brugada syndrome 1 +10 more | |
| | LOC110121269, SCN5A (R965L) | Single nucleotide variant (missense variant) | Brugada syndrome 1 +9 more | |
| | LOC110121269, SCN5A (Q960K) | Single nucleotide variant (missense variant) | Brugada syndrome 1 +9 more | |
| | LOC110121269, SCN5A (L939F) | Single nucleotide variant (missense variant) | Brugada syndrome +14 more | |