List of variants reported as likely pathogenic for cardiac conduction defect

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_002667.5(PLN):c.116T>G (p.Leu39Ter)	rs111033560	0.00002
NM_000257.4(MYH7):c.345+1G>A	rs112907315
NM_000335.5(SCN5A):c.5894C>G (p.Ser1965Cys)	rs1575703249
NM_000719.7(CACNA1C):c.32del (p.Pro11fs)	rs2052999161
NM_001035.3(RYR2):c.243G>A (p.Met81Ile)	rs1572627115
NM_001035.3(RYR2):c.9848T>A (p.Ile3283Asn)	rs1688456281
NM_001458.5(FLNC):c.5685del (p.Val1896fs)	rs1808809268
NM_001943.5(DSG2):c.2979G>T (p.Gln993His)	rs565904909

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