| Variation | | Type (Consequence) | Condition | Classification, Review status |
|---|
| | | Single nucleotide variant (intron variant) | Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome +2 more | |
| | | Single nucleotide variant (missense variant) | Catecholaminergic polymorphic ventricular tachycardia 1 +1 more | |
| | LOC126806068, RYR2 (K4223del) | Deletion (inframe_deletion) | Arrhythmogenic right ventricular dysplasia 2 +6 more | GConflicting classifications of pathogenicity |
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