List of variants reported as benign for atrial conduction disease

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_015978.3(TNNI3K):c.1027+33T>G	rs6424586	0.92549
NM_015978.3(TNNI3K):c.2431+30A>G	rs3895907	0.42662
NM_015978.3(TNNI3K):c.1825+13A>C	rs45589143	0.09225
NM_015978.3(TNNI3K):c.1773-20_1773-19insC	rs200033057	0.02220
NM_015978.3(TNNI3K):c.2057T>C (p.Ile686Thr)	rs3737564	0.00806
NM_015978.3(TNNI3K):c.334-8C>T	rs45443204	0.00528
NM_015978.3(TNNI3K):c.788C>T (p.Pro263Leu)	rs34521608	0.00128

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