| Variation | | Type (Consequence) | Condition | Classification, Review status |
---|
| | LOC126806067, RYR2 (S1295G) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +5 more | GConflicting classifications of pathogenicity |
| | | Single nucleotide variant (synonymous variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
Click to view in NCBI Gene