ClinVar Miner

List of variants reported as uncertain significance for Arrhythmogenic right ventricular dysplasia 2; Catecholaminergic polymorphic ventricular tachycardia 1; Ventricular arrhythmias due to cardiac ryanodine receptor calcium release deficiency syndrome by New York Genome Center

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.8437-1390C>T	rs1402357546	0.00006
NM_001035.3(RYR2):c.12667_12669del (p.Lys4223del)	rs794728838

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