List of variants reported as benign for Atrial conduction disease

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_015978.3(TNNI3K):c.1027+33T>G	rs6424586	0.92886
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.828-19A>C	rs17095165	0.01740
NM_015978.3(TNNI3K):c.2057T>C (p.Ile686Thr)	rs3737564	0.00979
NM_015978.3(TNNI3K):c.2181+20A>C	rs142942027	0.00540
NM_015978.3(TNNI3K):c.334-8C>T	rs45443204	0.00534
NM_015978.3(TNNI3K):c.969A>G (p.Lys323=)	rs141955645	0.00138
NM_015978.3(TNNI3K):c.788C>T (p.Pro263Leu)	rs34521608	0.00128
NM_015978.3(TNNI3K):c.1910C>T (p.Thr637Met)	rs2274260	0.00122
NM_015978.3(TNNI3K):c.827+11T>C	rs148757567	0.00102
NM_015978.3(TNNI3K):c.1878+10T>C	rs199892485	0.00038
NM_015978.3(TNNI3K):c.1620A>G (p.Gln540=)	rs55654209

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