| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Dilated Cardiomyopathy, Dominant +10 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (P1122L +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiac arrhythmia +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiac arrhythmia +12 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (A1121V +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiac arrhythmia +2 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (R1115W +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiac arrhythmia +10 more | |
| | LOC110121269, SCN5A (W1114* +1 more) | Single nucleotide variant (nonsense +1 more) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (D1113E +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiac arrhythmia +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +8 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (S1103Y +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +15 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (A1102T +1 more) | Single nucleotide variant (missense variant +1 more) | Sick sinus syndrome 1 +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +2 more | |
| | LOC110121269, SCN5A (A1099V +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +10 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (V1097M +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | LOC110121269, SCN5A (V1097L +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiac arrhythmia +10 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (W1094C +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (W1094C +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +1 more | |
| | LOC110121269, SCN5A (W1095* +1 more) | Single nucleotide variant (nonsense +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +2 more | |
| | LOC110121269, SCN5A (P1089L +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiac arrhythmia +13 more | |
| | LOC110121269, SCN5A (P1089T +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (A1087fs +1 more) | Deletion (frameshift variant +1 more) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (A1087T +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +10 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (P1085L +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiac arrhythmia +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiac arrhythmia +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | LOC110121269, SCN5A (Q1079E +1 more) | Single nucleotide variant (missense variant +2 more) | Cardiovascular phenotype +1 more | |
| | LOC110121269, SCN5A (S1078T +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +10 more | |
| | LOC110121269, SCN5A (K1075N) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | LOC110121269, SCN5A (E1072del) | Microsatellite (inframe_deletion) | not provided +3 more | |
| | LOC110121269, SCN5A (E1072S) | Inversion (missense variant) | Sick sinus syndrome 1 +10 more | |
| | LOC110121269, SCN5A (E1071K) | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +5 more | |
| | LOC110121269, SCN5A (T1069M) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +3 more | |
| | LOC110121269, SCN5A (E1064del) | Microsatellite (inframe_deletion) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +10 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +2 more | |
| | LOC110121269, SCN5A (E1053K) | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (P1048fs) | Indel (frameshift variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +3 more | |
| | LOC110121269, SCN5A (V1045M) | Single nucleotide variant (missense variant) | Brugada syndrome 1 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +2 more | |
| | LOC110121269, SCN5A (D1041N) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +1 more | |
| | LOC110121269, SCN5A (G1040R) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +2 more | |
| | LOC110121269, SCN5A (G1037S) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (G1035D) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +2 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +11 more | |
| | LOC110121269, SCN5A (E1029K) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 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) | Cardiovascular phenotype +10 more | |
| | LOC110121269, SCN5A (R1023P) | Single nucleotide variant (missense variant) | not provided +10 more | |
| | LOC110121269, SCN5A (R1023H) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (R1023C) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +3 more | |
| | LOC110121269, SCN5A (P1021S) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +4 more | |
| | LOC110121269, SCN5A (T1016M) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +2 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +3 more | |
| | LOC110121269, SCN5A (P1011L) | Single nucleotide variant (missense variant) | not specified +3 more | |
| | LOC110121269, SCN5A (P1008A) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (T1007I) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +2 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | LOC110121269, SCN5A (C1004R) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | LOC110121269, SCN5A (Q1000del) | Deletion (inframe_deletion) | Cardiovascular phenotype +3 more | |
| | LOC110121269, SCN5A (Q1000*) | Single nucleotide variant (nonsense) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (G999D) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (A996D) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +2 more | |
| | LOC110121269, SCN5A (A993T) | Single nucleotide variant (missense variant) | not specified +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiac arrhythmia +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | LOC110121269, SCN5A (R988Q) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +11 more | |
| | LOC110121269, SCN5A (R986W) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (G983D) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +2 more | |
| | LOC110121269, SCN5A (C982R) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +12 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (R975Q) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +10 more | |
| | LOC110121269, SCN5A (R971H) | Single nucleotide variant (missense variant) | Cardiac arrhythmia +2 more | |
| | LOC110121269, SCN5A (R965C) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (L961V) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (M956V) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | LOC110121269, SCN5A (E955fs) | Microsatellite (frameshift variant) | Cardiac arrhythmia +5 more | GConflicting classifications of pathogenicity |
| | LOC110121269, SCN5A (D953E) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |