| | CCDC146, CCDC201 +4735 more | Copy number loss | See cases | |
| | | Copy number loss | See cases | |
| | AKAP9, LOC129998788 +1 more | Copy number gain | See cases | |
| | | Duplication | not provided | |
| | | Single nucleotide variant | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided | |
| | | Microsatellite (5 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Congenital long QT syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Congenital long QT syndrome +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Congenital long QT syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Congenital long QT syndrome | |
| | | Single nucleotide variant (5 prime UTR variant) | Congenital long QT syndrome | |
| | | Duplication | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | AKAP9, LOC129998788 (L10P) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | AKAP9, LOC129998788 (E11G) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | AKAP9, LOC129998788 (A12T) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | AKAP9, LOC129998788 (G13S) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +1 more | GConflicting classifications of pathogenicity |
| | AKAP9, LOC129998788 (K14T) | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | AKAP9, LOC129998788 (A15V) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Microsatellite (intron variant) | Long QT syndrome | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome +3 more | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Copy number gain | See cases | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome +1 more | |
| | | Deletion (genic upstream transcript variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (nonsense) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Ventricular tachycardia | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | not specified +9 more | |
| | | Indel (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Microsatellite (frameshift variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Congenital long QT syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome 11 +2 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | AKAP9-related condition +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Microsatellite (splice donor variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |