| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861897, MHRT
+2 more (S1648fs) | Deletion (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy 1 | |
| | | Single nucleotide variant (missense variant) | Myosin storage myopathy +7 more | |
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