| | | Single nucleotide variant (3 prime UTR variant) | Primary dilated cardiomyopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Primary dilated cardiomyopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Primary dilated cardiomyopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Primary dilated cardiomyopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Primary dilated cardiomyopathy | |
| | | Duplication (3 prime UTR variant) | Dilated Cardiomyopathy, Dominant +1 more | |
| | | Duplication (3 prime UTR variant) | Dilated Cardiomyopathy, Dominant +1 more | |
| | | Deletion (3 prime UTR variant) | Dilated Cardiomyopathy, Dominant | |
| | | Deletion (3 prime UTR variant) | Dilated Cardiomyopathy, Dominant | |
| | | Single nucleotide variant (3 prime UTR variant) | Primary dilated cardiomyopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Primary dilated cardiomyopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Primary dilated cardiomyopathy +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Primary dilated cardiomyopathy | |
| | | Microsatellite (3 prime UTR variant) | Dilated Cardiomyopathy, Dominant | |
| | | Single nucleotide variant (3 prime UTR variant) | Primary dilated cardiomyopathy +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (nonsense) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | ANKRD1-related dilated cardiomyopathy +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | ANKRD1-related dilated cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related disorder +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (synonymous variant) | ANKRD1-related dilated cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | ANKRD1-related dilated cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (intron variant) | not specified | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | not provided | |
| | | Single nucleotide variant (intron variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Duplication (splice donor variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (splice donor variant) | ANKRD1-related dilated cardiomyopathy +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | not provided +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (synonymous variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy +2 more | |
| | | Single nucleotide variant (nonsense) | not specified +2 more | |
| | | Duplication (nonsense +1 more) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | Primary dilated cardiomyopathy | |
| | | Deletion (nonsense) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
| | | Duplication (nonsense) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy +1 more | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (synonymous variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Deletion (frameshift variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +1 more | |
| | | Single nucleotide variant (intron variant) | ANKRD1-related dilated cardiomyopathy | |
| | | Single nucleotide variant (intron variant) | Cardiovascular phenotype +1 more | |