| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | Short QT syndrome type 2 +5 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +4 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Short QT syndrome type 2 +5 more | GConflicting classifications of pathogenicity |
| | | Deletion (5 prime UTR variant) | not specified | |
| | | Single nucleotide variant (5 prime UTR variant) | Congenital long QT syndrome +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (5 prime UTR variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (5 prime UTR variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital long QT syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Congenital long QT syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 1 | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Deletion (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Jervell and Lange-Nielsen syndrome 1 +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Jervell and Lange-Nielsen syndrome 1 +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Familial atrial fibrillation +4 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 1 +7 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | | Deletion (frameshift variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (nonsense) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Congenital long QT syndrome +4 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Conduction disorder of the heart +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (nonsense) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (nonsense +1 more) | Congenital long QT syndrome +1 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Duplication (frameshift variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | not provided +3 more | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (nonsense) | Jervell and Lange-Nielsen syndrome 1 | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (nonsense) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | not provided | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant +1 more) | not specified | |
| | | Duplication (inframe_insertion +1 more) | Long QT syndrome | |
| | | Duplication (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Atrial fibrillation, familial, 3 +8 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Duplication (frameshift variant) | Long QT syndrome 1 | |
| | | Microsatellite (inframe_indel +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | | Duplication (inframe_insertion) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (nonsense) | Cardiac arrhythmia +1 more | |
| | | Single nucleotide variant (nonsense) | Cardiovascular phenotype +4 more | GPathogenic/Likely pathogenic |
| | | Deletion (frameshift variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +2 more | |
| | | Insertion (inframe_indel) | not provided | |
| | | Single nucleotide variant (synonymous variant +1 more) | not provided | |
| | | Deletion (frameshift variant) | Cardiac arrhythmia +1 more | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Insertion (inframe_indel) | not provided | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Congenital long QT syndrome | |
| | | Single nucleotide variant (synonymous variant +1 more) | Long QT syndrome | |