List of variants reported as uncertain significance for ventricular tachycardia by Clinical Genomics Laboratory, Stanford Medicine

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.3484G>A (p.Val1162Met)	rs377030538	0.00002
NM_001035.3(RYR2):c.12752A>G (p.Asn4251Ser)	rs750064223	0.00001
NM_001035.3(RYR2):c.14151+1G>A	rs745576995	0.00001
NM_001035.3(RYR2):c.1573T>G (p.Ser525Ala)	rs1207389001	0.00001
NM_001232.4(CASQ2):c.172G>A (p.Glu58Lys)	rs376824588	0.00001

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