| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861898, MYH7 (R870C) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | LOC126861898, MYH7 (A797T) | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +18 more | GPathogenic/Likely pathogenic |
| | LOC126861898, MYH7 (R787H) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | LOC126861898, MYH7 (R787C) | Single nucleotide variant (missense variant) | Cardiomyopathy +7 more | GConflicting classifications of pathogenicity |
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