List of variants reported as likely benign for cardiac rhythm disease by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_006073.4(TRDN):c.1538-13T>G	rs55704802	0.00651
NM_002234.4(KCNA5):c.1733G>A (p.Arg578Lys)	rs12720445	0.00612
NM_002234.4(KCNA5):c.929C>T (p.Pro310Leu)	rs17215402	0.00439
NM_002234.4(KCNA5):c.919C>T (p.Pro307Ser)	rs17215409	0.00241
NM_006073.4(TRDN):c.793+61T>C	rs572614305	0.00177
NM_017636.4(TRPM4):c.246G>T (p.Gly82=)	rs756668921	0.00006
NM_002234.4(KCNA5):c.1641G>T (p.Gly547=)	rs1278466330
NM_006073.4(TRDN):c.1672+6T>C
NM_006073.4(TRDN):c.1721-4A>T	rs60743141
NM_006073.4(TRDN):c.425-11dup	rs950851610
NM_006073.4(TRDN):c.931+18del	rs201431159
NM_017636.4(TRPM4):c.2529G>A (p.Gly843=)	rs754769591
NM_017636.4(TRPM4):c.2778+8del	rs1600513831

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