List of variants reported as likely benign for heart conduction disease by Genomic Diagnostic Laboratory, Division of Genomic Diagnostics, Children's Hospital of Philadelphia

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.1571C>A (p.Ser524Tyr)	rs41313691	0.01184
NM_000335.5(SCN5A):c.6007T>C (p.Phe2003Leu)	rs41311117	0.00192
NM_001035.3(RYR2):c.9560A>G (p.Lys3187Arg)	rs184218219	0.00137

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