| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861896, MYH6 (R1664H) | Single nucleotide variant (missense variant) | Cardiomyopathy +7 more | GConflicting classifications of pathogenicity |
| | LOC126861896, MYH6 (E1640K) | Single nucleotide variant (missense variant) | Primary familial hypertrophic cardiomyopathy +7 more | |
| | LOC126861896, MYH6 (K1619R) | Single nucleotide variant (missense variant) | not provided | |
| | MYH6, LOC126861896 (R1610C) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +7 more | |
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