C1631597[trait identifier] AND "KardioGenetik, Herz- und Diabeteszentr - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 640529	NM_001035.3(RYR2):c.782A>G (p.His261Arg)	RYR2 (H261R)	Single nucleotide variant (missense variant)	Arrhythmogenic right ventricular dysplasia 2 +5 more	GUncertain significance
Select item 201215	NM_001035.3(RYR2):c.1259G>A (p.Arg420Gln)	RYR2 (R420Q)	Single nucleotide variant (missense variant)	not provided +2 more	GPathogenic
Select item 43765	NM_001035.3(RYR2):c.3152G>A (p.Arg1051His)	RYR2 (R1051H)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +5 more	GConflicting classifications of pathogenicity
Select item 1021015	NM_001035.3(RYR2):c.12334G>A (p.Asp4112Asn)	RYR2 (D4112N)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1	GPathogenic/Likely pathogenic
Select item 2743511	NM_001035.3(RYR2):c.14550CTT[2] (p.Phe4853del)	RYR2 (F4853del)	Microsatellite (inframe_deletion)	Catecholaminergic polymorphic ventricular tachycardia 1 +1 more	GUncertain significance
Select item 229345	NM_006073.4(TRDN):c.1367A>G (p.Gln456Arg)	TRDN (Q456R +1 more)	Single nucleotide variant (missense variant)	Catecholaminergic polymorphic ventricular tachycardia 1 +4 more	GConflicting classifications of pathogenicity

ClinVar