| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861898, MYH7 (R858C) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 +10 more | GPathogenic/Likely pathogenic |
| | LOC126861898, MYH7 (A797T) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +18 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene