| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861898, MYH7 (M877T) | Single nucleotide variant (missense variant) | Arrhythmogenic cardiomyopathy | |
| | LOC126861898, MYH7 (R870H) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
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