| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | LOC126806068, RYR2 (I4173M) | Single nucleotide variant (missense variant) | Catecholaminergic polymorphic ventricular tachycardia +1 more | |
| | | Single nucleotide variant (synonymous variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +5 more | GConflicting classifications of pathogenicity |
| | LOC126806068, RYR2 (T4281M) | Single nucleotide variant (missense variant) | not provided +3 more | |
| | LOC126806068, RYR2 (R4307C) | Single nucleotide variant (missense variant) | Cardiovascular phenotype +6 more | GConflicting classifications of pathogenicity |
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