List of variants reported as uncertain significance for Catecholaminergic polymorphic ventricular tachycardia 1 by Center For Human Genetics And Laboratory Diagnostics, Dr. Klein, Dr. Rost And Colleagues

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_001035.3(RYR2):c.3152G>A (p.Arg1051His)	rs79457258	0.00014
NM_001035.3(RYR2):c.1511G>A (p.Arg504His)	rs201600087	0.00006
NM_001035.3(RYR2):c.5096G>A (p.Arg1699His)	rs779464111	0.00002
NM_001035.3(RYR2):c.10241G>A (p.Arg3414Lys)	rs1131692324
NM_001035.3(RYR2):c.11144A>G (p.Glu3715Gly)	rs1573761441
NM_001035.3(RYR2):c.11234G>T (p.Ser3745Ile)	rs1573821691
NM_001035.3(RYR2):c.1918A>G (p.Arg640Gly)	rs886041109
NM_001035.3(RYR2):c.2468A>T (p.Tyr823Phe)	rs759178071
NM_001035.3(RYR2):c.3257G>A (p.Arg1086Gln)	rs749566870
NM_001035.3(RYR2):c.326G>A (p.Gly109Asp)	rs1572014527
NM_001035.3(RYR2):c.5585A>G (p.Asp1862Gly)	rs1559117209
NM_001035.3(RYR2):c.6394G>C (p.Val2132Leu)	rs1553531684
NM_001035.3(RYR2):c.6520G>T (p.Val2174Phe)	rs1131692321
NM_001035.3(RYR2):c.7469T>C (p.Val2490Ala)	rs886041112
NM_001035.3(RYR2):c.94C>A (p.Gln32Lys)	rs1553373926

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