| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | MYH6, LOC114827851 (A110V) | Single nucleotide variant (missense variant) | not provided +2 more | |
| | | Single nucleotide variant (synonymous variant) | Hypertrophic cardiomyopathy 14 +1 more | GConflicting classifications of pathogenicity |
| | LOC114827851, MYH6 (F31fs) | Deletion (frameshift variant) | not provided | |
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