| | | Single nucleotide variant (missense variant) | Long QT syndrome +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 1 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Caveolinopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Caveolinopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 1 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Caveolinopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Caveolinopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Caveolinopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Caveolinopathy | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 1 +5 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Caveolinopathy +1 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not provided +3 more | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | Caveolinopathy | |
| | | Single nucleotide variant (3 prime UTR variant +1 more) | not specified +1 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +7 more | |
| | | Deletion (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Caveolinopathy +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +4 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Caveolinopathy +7 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +3 more | |
| | | Single nucleotide variant (missense variant) | Limb-Girdle Muscular Dystrophy, Dominant +2 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +10 more | |
| | | Single nucleotide variant (synonymous variant) | Long QT syndrome +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Congenital long QT syndrome +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Caveolinopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +3 more | |
| | | Single nucleotide variant (synonymous variant) | Caveolinopathy +5 more | |
| | | Single nucleotide variant (synonymous variant) | Rippling muscle disease 2 +8 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +6 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +6 more | |
| | | Single nucleotide variant (synonymous variant) | Caveolinopathy +6 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Limb-Girdle Muscular Dystrophy, Dominant +3 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Congenital long QT syndrome +3 more | |
| | | Single nucleotide variant (missense variant) | CAV3-related disorder +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Caveolinopathy | |
| | | Single nucleotide variant (missense variant) | CAV3-related disorder +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +13 more | |