| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | AKAP9, LOC129998788 (A15V) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | AKAP9, LOC121175350 (E1651D) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | AKAP9, LOC129998789 (L271V) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | AKAP9, LOC121175350 (S1642F) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Inborn genetic diseases | |
| | AKAP9, LOC129998789 (Q265H) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 11 | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 11 | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 11 | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | AKAP9, LOC121175350 (E1672K) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | AKAP9, LOC121175350 (N1680S) | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | AKAP9, LOC129998789 (Q268E) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | | Single nucleotide variant (splice donor variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | AKAP9, LOC129998789 (A261T) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | AKAP9, LOC129998789 (R252fs) | Duplication (frameshift variant) | Cardiovascular phenotype | |
| | AKAP9, LOC129998789 (L251fs) | Microsatellite (frameshift variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype | |
| | AKAP9, LOC121175350 (L1657S) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | AKAP9, LOC121175350 (E1653D) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | AKAP9, LOC121175350 (I1643M) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | AKAP9, LOC129998788 (G13S) | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | AKAP9, LOC129998789 (A247G) | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | AKAP9, LOC121175350 (Q1665H) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | AKAP9, LOC121175350 (S1667P) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | AKAP9, LOC121175350 (Q1686E) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | AKAP9, LOC121175350 (E1651G) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +1 more | GConflicting classifications of pathogenicity |
| | AKAP9, LOC121175350 (T1683R) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Microsatellite (intron variant) | Long QT syndrome | |
| | AKAP9, LOC129998788 (E11G) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | AKAP9, LOC129998789 (Q265E) | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | AKAP9, LOC121175350 (V1655fs) | Deletion (frameshift variant) | Long QT syndrome | |
| | AKAP9, LOC129998788 (L10P) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome | |
| | AKAP9, LOC121175350 (V1649I) | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | AKAP9, LOC129998789 (L251R) | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (intron variant) | not specified +3 more | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 11 | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 11 | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 11 | |
| | | Single nucleotide variant (missense variant) | Long QT syndrome 11 | |
| | | Deletion (splice acceptor variant) | not provided | |
| | AKAP9, LOC121175350 (R1679H) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | GConflicting classifications of pathogenicity |
| | AKAP9, LOC121175350 (R1654S) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | AKAP9, LOC121175350 (Q1665L) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | GConflicting classifications of pathogenicity |
| | AKAP9, LOC121175350 (R1679C) | Single nucleotide variant (missense variant) | Long QT syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | not provided | |
| | | Copy number loss | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Copy number gain | not provided | |
| | | Single nucleotide variant (intron variant) | Long QT syndrome | |
| | AKAP9, LOC129998788 (A12T) | Single nucleotide variant (missense variant) | Long QT syndrome | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | LOC121175350, AKAP9 (I1643V) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Microsatellite (intron variant) | Long QT syndrome | |
| | AKAP9, LOC129998788 (K14T) | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | AKAP9, LOC121175350 (T1683M) | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | |
| | | Single nucleotide variant (intron variant) | not specified +2 more | |
| | AKAP9, LOC121175350 (A1662V) | Single nucleotide variant (missense variant) | AKAP9-related condition +4 more | GConflicting classifications of pathogenicity |
| | LOC121175350, AKAP9 (I1643L) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Copy number gain | See cases | |