| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861897, MYH7 (L1769M) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | LOC126861897, MHRT
+1 more (R1662H) | Single nucleotide variant (non-coding transcript variant +1 more) | not provided +4 more | GConflicting classifications of pathogenicity |
| | LOC126861897, MHRT
+1 more (A1637T) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiomyopathy | |
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