| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +4 more | |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy | |
| | LOC126861898, MYH7 (A797T) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +18 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy | |
Click to view in NCBI Gene