| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861898, MYH7 (R870H) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | LOC126861898, MYH7 (L859P) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | LOC126861898, MYH7 (R858C) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 +10 more | GPathogenic/Likely pathogenic |
| | LOC126861898, MYH7 (D778E) | Single nucleotide variant (missense variant) | not provided +3 more | GPathogenic/Likely pathogenic |
Click to view in NCBI Gene