| | | Single nucleotide variant (5 prime UTR variant +2 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (intron variant +1 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (M1L +1 more) | Single nucleotide variant (missense variant +2 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (T102N) | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +1 more | |
| | LOC126861356, SCN4B (V42A +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | LOC126861356, SCN4B (E81L) | Indel (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (K88N) | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (R100S) | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome 10 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (T126M +1 more) | Single nucleotide variant (missense variant +1 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | Cardiovascular phenotype | |
| | LOC126861356, SCN4B (D43G +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | SCN4B, LOC126861356 (V151I +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | LOC126861356, SCN4B (I147F +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype | |
| | LOC126861356, SCN4B (H132R +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | LOC126861356, SCN4B (D125H +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | LOC126861356, SCN4B (F123Y +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | LOC126861356, SCN4B (N112K +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Cardiovascular phenotype | |
| | LOC126861356, SCN4B (A145T +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (E87K) | Single nucleotide variant (missense variant +3 more) | Cardiovascular phenotype +1 more | |
| | LOC126861356, SCN4B (P91H) | Single nucleotide variant (missense variant +3 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome 10 +1 more | GConflicting classifications of pathogenicity |
| | LOC126861356, SCN4B (I116fs +1 more) | Deletion (frameshift variant +1 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome 10 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided +1 more | |
| | LOC126861356, SCN4B (I116T +1 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (S89C) | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (K96E) | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (D125N +1 more) | Single nucleotide variant (missense variant +1 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (R100P) | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (D120G +1 more) | Single nucleotide variant (missense variant +1 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome 10 +1 more | |
| | LOC126861356, SCN4B (L8P +1 more) | Single nucleotide variant (missense variant +1 more) | Long QT syndrome 10 | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Long QT syndrome 10 | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | LOC126861356, SCN4B (R100H) | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (R100C) | Single nucleotide variant (missense variant +3 more) | Long QT syndrome 10 +1 more | |
| | LOC126861356, SCN4B (T126A +1 more) | Single nucleotide variant (intron variant +1 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (N113del +1 more) | Microsatellite (inframe_deletion +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +2 more | |
| | LOC126861356, SCN4B (V133M +1 more) | Single nucleotide variant (intron variant +1 more) | Long QT syndrome 10 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not specified +1 more | |
| | | Single nucleotide variant (5 prime UTR variant +2 more) | not provided +1 more | |
| | LOC126861356, SCN4B (P91T) | Single nucleotide variant (5 prime UTR variant +3 more) | Primary dilated cardiomyopathy | |
| | LOC126861356, SCN4B (L121P +1 more) | Single nucleotide variant (missense variant +1 more) | Congenital long QT syndrome +1 more | |
| | LOC126861356, SCN4B (I80T) | Single nucleotide variant (5 prime UTR variant +3 more) | Long QT syndrome 10 | |
| | LOC126861356, SCN4B (V152I +1 more) | Single nucleotide variant (missense variant +1 more) | not provided +2 more | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | SCN4B, LOC126861356 (T94M) | Single nucleotide variant (5 prime UTR variant +3 more) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (intron variant) | not specified +1 more | GConflicting classifications of pathogenicity |