List of variants reported as likely benign for Primary dilated cardiomyopathy by Illumina Laboratory Services, Illumina

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Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_014391.3(ANKRD1):c.346-15T>A	rs11595794	0.01808
NM_000116.5(TAFAZZIN):c.383T>C (p.Phe128Ser)	rs146934311	0.01627
NM_014391.3(ANKRD1):c.*366G>A	rs17102330	0.01092
NM_000116.5(TAFAZZIN):c.-88G>C	rs113130344	0.01005
NM_014391.3(ANKRD1):c.-17A>G	rs79341122	0.00753
NM_014391.3(ANKRD1):c.*41T>G	rs150520404	0.00731
NM_014391.3(ANKRD1):c.-34C>T	rs114144205	0.00491
NM_014391.3(ANKRD1):c.*588A>C	rs137950655	0.00483
NM_014391.3(ANKRD1):c.148G>C (p.Ala50Pro)	rs28730751	0.00387
NM_000116.5(TAFAZZIN):c.873G>A (p.Gly291=)	rs35902788	0.00367
NM_014391.3(ANKRD1):c.827C>T (p.Ala276Val)	rs35550482	0.00244
NM_000116.5(TAFAZZIN):c.646+14C>T	rs191527230	0.00206
NM_000116.5(TAFAZZIN):c.*560G>A	rs782808430	0.00093
NM_000116.5(TAFAZZIN):c.*396C>T	rs144283894	0.00036
NM_014391.3(ANKRD1):c.108T>C (p.Ala36=)	rs145211719	0.00009
NM_000116.5(TAFAZZIN):c.675G>A (p.Pro225=)	rs201046790	0.00001
NM_014391.3(ANKRD1):c.196C>G (p.Arg66Gly)	rs397517249

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