| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861896, MYH6 (R1691H) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy +8 more | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +7 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 +7 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 14 +7 more | |
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