List of variants reported as benign for not specified by Stanford Center for Inherited Cardiovascular Disease, Stanford University

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_000363.5(TNNI3):c.25-8T>A	rs3729836	0.35138
NM_000238.4(KCNH2):c.2690A>C (p.Lys897Thr)	rs1805123	0.20300
NM_001035.3(RYR2):c.4198A>G (p.Ser1400Gly)	rs56229512	0.01531
NM_001005242.3(PKP2):c.76G>A (p.Asp26Asn)	rs143004808	0.00716
NM_001032283.3(TMPO):c.565+2487C>T	rs17028450	0.00576
NM_002294.3(LAMP2):c.1093+2514G>A	rs144140265	0.00404
NM_000238.4(KCNH2):c.1039C>T (p.Pro347Ser)	rs138776684	0.00061
NM_174934.4(SCN4B):c.22G>A (p.Gly8Ser)	rs149868494	0.00009
NM_000335.5(SCN5A):c.52C>T (p.Arg18Trp)	rs199473044	0.00006
NM_004415.4(DSP):c.4741A>G (p.Lys1581Glu)	rs186842903	0.00003
NM_174936.4(PCSK9):c.45GCT[8] (p.Leu23dup)	rs35574083

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