| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (missense variant) | not provided +3 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | not specified +4 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | MYL2, LOC114827850 (F18fs) | Deletion (frameshift variant) | Hypertrophic cardiomyopathy 10 +1 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene