| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +2 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | LOC126861896, MYH6 (R1664H) | Single nucleotide variant (missense variant) | not provided +7 more | GConflicting classifications of pathogenicity |
| | LOC126861896, MYH6 (E1640K) | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +7 more | |
| | LOC126861896, MYH6 (K1619R) | Single nucleotide variant (missense variant) | not provided | |
| | LOC126861896, MYH6 (R1610C) | Single nucleotide variant (missense variant) | Atrial septal defect 3 +8 more | |
| | | Microsatellite (frameshift variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +10 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 +6 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +9 more | |
| | | Single nucleotide variant (missense variant) | Atrial septal defect 3 +7 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +7 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +4 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +6 more | |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +2 more | |
| | | Single nucleotide variant (splice donor variant) | Hypertrophic cardiomyopathy 14 +7 more | |
| | | Single nucleotide variant (missense variant) | not provided +1 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +1 more | |
| | | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1EE +5 more | |
| | | Indel (missense variant) | Hypertrophic cardiomyopathy 14 +1 more | |
| | | Single nucleotide variant (nonsense) | Hypertrophic cardiomyopathy 14 +1 more | |
| | | Single nucleotide variant (missense variant) | not provided +6 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (missense variant) | not provided | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GConflicting classifications of pathogenicity |
| | MYH6, LOC114827851 (A110V) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 14 +1 more | GConflicting classifications of pathogenicity |
| | LOC114827851, MYH6 (F31fs) | Deletion (frameshift variant) | not provided | |