| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861897, MYH7 (M1765K) | Single nucleotide variant (missense variant) | Cardiomyopathy +1 more | |
| | LOC126861897, MHRT
+1 more (I1707V) | Single nucleotide variant (non-coding transcript variant +1 more) | Pericarditis | |
| | LOC126861897, MHRT
+1 more (V1674M) | Single nucleotide variant (non-coding transcript variant +1 more) | Hypertrophic cardiomyopathy +2 more | |
Click to view in NCBI Gene