| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Duplication (3 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Duplication (3 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Deletion (3 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Duplication (3 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Indel (3 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Deletion (3 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Wolff-Parkinson-White pattern +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Deletion (3 prime UTR variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Wolff-Parkinson-White pattern +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (3 prime UTR variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (3 prime UTR variant) | not specified +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not specified +7 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 6 +7 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 6 +7 more | |
| | | Single nucleotide variant (intron variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +8 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 6 +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 6 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 6 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Cardiomyopathy +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | PRKAG2-related condition +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +7 more | GConflicting classifications of pathogenicity |
| | LOC129999660, PRKAG2 (A233G +2 more) | Single nucleotide variant (missense variant +1 more) | Cardiovascular phenotype +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Wolff-Parkinson-White pattern +4 more | |
| | | Duplication (frameshift variant) | Cardiovascular phenotype +4 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 6 +5 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 6 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Congestive heart failure +8 more | |
| | | Single nucleotide variant (synonymous variant) | Cardiomyopathy +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 6 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Wolff-Parkinson-White pattern +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 6 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 6 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Wolff-Parkinson-White pattern +7 more | |
| | | Single nucleotide variant (missense variant) | not specified +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (intron variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | not specified +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant +1 more) | Hypertrophic cardiomyopathy +4 more | |
| | | Single nucleotide variant (intron variant) | Hypertrophic cardiomyopathy 6 +4 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 6 +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +2 more | |
| | | Single nucleotide variant (synonymous variant) | Lethal congenital glycogen storage disease of heart +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +2 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +4 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | not provided +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (5 prime UTR variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Single nucleotide variant (5 prime UTR variant) | Wolff-Parkinson-White pattern +2 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy 6 +1 more | |
| | | Single nucleotide variant (non-coding transcript variant) | Familial Hypertrophic Cardiomyopathy with Wolff-Parkinson-White Syndrome +2 more | |
| | | Single nucleotide variant (non-coding transcript variant) | not provided +2 more | GConflicting classifications of pathogenicity |