| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126861897, MYH7 (T1760R) | Single nucleotide variant (missense variant) | Hypertrophic cardiomyopathy 1 | |
| | LOC126861897, MHRT
+1 more (K1729del) | Microsatellite (non-coding transcript variant +1 more) | Cardiovascular phenotype +2 more | |
Click to view in NCBI Gene