| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861897, MHRT
+1 more (R1608H) | Single nucleotide variant (non-coding transcript variant +1 more) | Cardiovascular phenotype +3 more | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
| | | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy | |
Click to view in NCBI Gene