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

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Total variants: 3

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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.1772G>C (p.Ser591Thr)	rs145260115	0.00116
NM_015978.3(TNNI3K):c.720_721insGGGACTCCAT (p.Phe241fs)	rs556027408

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