"Clinical Genetics, Academic Medical Center"[submitter] AND "LOC126806 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 138943	NM_001035.3(RYR2):c.3888C>T (p.Asn1296=)	LOC126806067, RYR2	Single nucleotide variant (synonymous variant)	RYR2-related disorder +6 more	GConflicting classifications of pathogenicity
Select item 1284371	NM_001035.3(RYR2):c.4148G>A (p.Arg1383His)	LOC126806067, RYR2 (R1383H)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia +3 more	GConflicting classifications of pathogenicity