| | | Single nucleotide variant (3 prime UTR variant) | Sacral defect with anterior meningocele +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sacral defect with anterior meningocele +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sacral defect with anterior meningocele +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sacral defect with anterior meningocele +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sacral defect with anterior meningocele +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sacral defect with anterior meningocele +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sacral defect with anterior meningocele +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Catecholaminergic polymorphic ventricular tachycardia +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sacral defect with anterior meningocele +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sacral defect with anterior meningocele +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Sacral defect with anterior meningocele +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Catecholaminergic polymorphic ventricular tachycardia +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Catecholaminergic polymorphic ventricular tachycardia +2 more | |
| | | Duplication (3 prime UTR variant) | Caudal regression sequence +2 more | |
| | | Microsatellite (3 prime UTR variant) | Catecholaminergic polymorphic ventricular tachycardia | |
| | | Deletion (3 prime UTR variant) | Caudal regression sequence +2 more | |
| | | Duplication (3 prime UTR variant) | Catecholaminergic polymorphic ventricular tachycardia | |
| | | Deletion (3 prime UTR variant) | Caudal regression sequence +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Caudal regression sequence +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Catecholaminergic polymorphic ventricular tachycardia 2 +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Caudal regression sequence +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +4 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +7 more | |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia +6 more | |
| | | Microsatellite (inframe_deletion) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +7 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +8 more | |
| | | Single nucleotide variant (intron variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Microsatellite | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite | Catecholaminergic polymorphic ventricular tachycardia | |
| | | Microsatellite | Catecholaminergic polymorphic ventricular tachycardia 2 +2 more | |
| | | Microsatellite | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Microsatellite | Catecholaminergic polymorphic ventricular tachycardia +2 more | |
| | | Microsatellite | Catecholaminergic polymorphic ventricular tachycardia +2 more | |
| | | Indel | Catecholaminergic polymorphic ventricular tachycardia +2 more | |
| | | Single nucleotide variant | Catecholaminergic polymorphic ventricular tachycardia 2 +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Catecholaminergic polymorphic ventricular tachycardia +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Catecholaminergic polymorphic ventricular tachycardia +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Arrhythmogenic right ventricular dysplasia 2 +3 more | |
| | | Single nucleotide variant (intron variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +6 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | not provided +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +7 more | |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +6 more | |
| | | Single nucleotide variant (intron variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +3 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +6 more | |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Arrhythmogenic right ventricular dysplasia 2 +2 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Catecholaminergic polymorphic ventricular tachycardia +1 more | |
| | | Single nucleotide variant (intron variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +6 more | |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 2 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (synonymous variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +7 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +7 more | |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Arrhythmogenic right ventricular dysplasia 2 +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | |
| | | Single nucleotide variant (missense variant) | Catecholaminergic polymorphic ventricular tachycardia +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Arrhythmogenic right ventricular dysplasia 2 +5 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | LOC126806067, RYR2 (M1300L) | Single nucleotide variant (missense variant) | Catecholaminergic polymorphic ventricular tachycardia +2 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | LOC126806067, RYR2 (D1357H) | Single nucleotide variant (missense variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | |
| | | Single nucleotide variant (missense variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +3 more | |
| | | Single nucleotide variant (missense variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +6 more | GConflicting classifications of pathogenicity |
| | | Deletion | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +6 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia +6 more | GConflicting classifications of pathogenicity |