| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861898, MYH7 (R869C) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | GPathogenic/Likely pathogenic |
| | LOC126861898, MYH7 (A797T) | Single nucleotide variant (missense variant) | MYH7-related disorder +18 more | GPathogenic/Likely pathogenic |
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