| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Deletion (frameshift variant) | Hypertrophic cardiomyopathy 14 | |
| | LOC126861896, MYH6 (S1598L) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiomyopathy +3 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 | |
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