| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126861897, MYH7 (A1763T) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 +11 more | |
| | LOC126861897, MYH7 (T1760M) | Single nucleotide variant (missense variant) | Myopathy, myosin storage, autosomal recessive +9 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (non-coding transcript variant +1 more) | Left ventricular noncompaction cardiomyopathy +13 more | |
| | | Single nucleotide variant (splice acceptor variant) | Hypertrophic cardiomyopathy +10 more | GConflicting classifications of pathogenicity |
| | LOC126861898, MYH7 (R858C) | Single nucleotide variant (missense variant) | not provided +10 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | not provided +9 more | GPathogenic/Likely pathogenic |
| | | Single nucleotide variant (missense variant) | Myopathy, myosin storage, autosomal recessive +5 more | GConflicting classifications of pathogenicity |
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