List of variants reported as likely pathogenic for heart conduction disease by Genetics and Molecular Pathology, SA Pathology

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000335.5(SCN5A):c.2678G>A (p.Arg893His)	rs199473172	0.00001
NM_000335.5(SCN5A):c.5620_5622dup (p.Met1874dup)	rs1474459822
NM_170707.4(LMNA):c.324del (p.Val109fs)

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