| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +5 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +7 more | |
| | LOC126861897, MYH7 (C1748Y) | Single nucleotide variant (missense variant) | Dilated cardiomyopathy 1S +8 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +8 more | |
| | | Single nucleotide variant (synonymous variant) | not specified +1 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene