List of variants reported as likely benign for Atrial conduction disease

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_015978.3(TNNI3K):c.512T>C (p.Leu171Ser)	rs6685961	0.00169
NM_015978.3(TNNI3K):c.969A>G (p.Lys323=)	rs141955645	0.00138
NM_015978.3(TNNI3K):c.1772G>C (p.Ser591Thr)	rs145260115	0.00116
NM_015978.3(TNNI3K):c.1550A>G (p.Asn517Ser)	rs138357965	0.00025
NM_015978.3(TNNI3K):c.193G>T (p.Glu65Ter)	rs201061482	0.00008
NM_015978.3(TNNI3K):c.720_721insGGGACTCCAT (p.Phe241fs)	rs556027408

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