| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | | Single nucleotide variant (missense variant) | MYH6-related cardiac defects +2 more | |
| | | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | |
| | | Single nucleotide variant (missense variant) | not provided +8 more | |
| | | Single nucleotide variant (missense variant) | Atrial septal defect 3 +5 more | |
| | | Single nucleotide variant (nonsense) | not provided +5 more | |
| | LOC114827851, MYH6 (M165L) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 +6 more | |
| | LOC114827851, MYH6 (N160D) | Single nucleotide variant (missense variant) | Atrial septal defect 3 +2 more | |
Click to view in NCBI Gene