| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | LOC126861898, MYH7 (R869H) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | MYH7-related disorder +2 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene