List of variants reported as benign for Dilated Cardiomyopathy, Dominant by Invitae

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Total variants: 22

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HGVS	dbSNP	gnomAD frequency
NM_001006630.2(CHRM2):c.*295T>A	rs8191992	0.59512
NM_001330.5(CTF1):c.26-1030C>G	rs11862962	0.23264
NM_001330.5(CTF1):c.120C>T (p.Tyr40=)	rs8059269	0.02315
NM_201550.4(LRRC10):c.360C>T (p.Leu120=)	rs145823585	0.00793
NM_001006630.2(CHRM2):c.1197T>C (p.Thr399=)	rs34586275	0.00676
NM_201550.4(LRRC10):c.584T>C (p.Ile195Thr)	rs151080979	0.00397
NM_001006630.2(CHRM2):c.691G>A (p.Val231Ile)	rs76394680	0.00359
NM_201550.4(LRRC10):c.521T>C (p.Leu174Pro)	rs146361892	0.00196
NM_001006630.2(CHRM2):c.773A>G (p.Asn258Ser)	rs142006633	0.00128
NM_001006630.2(CHRM2):c.1050A>G (p.Ser350=)	rs60372903	0.00070
NM_001006630.2(CHRM2):c.991A>T (p.Thr331Ser)	rs146328962	0.00064
NM_001330.5(CTF1):c.274G>A (p.Ala92Thr)	rs2234933	0.00062
NM_201550.4(LRRC10):c.768G>A (p.Ala256=)	rs148566929	0.00056
NM_201550.4(LRRC10):c.453C>T (p.Ala151=)	rs12229290	0.00050
NM_001006630.2(CHRM2):c.456C>T (p.Phe152=)	rs148163637	0.00038
NM_001006630.2(CHRM2):c.549T>C (p.Asn183=)	rs141951417	0.00031
NM_201550.4(LRRC10):c.206C>T (p.Pro69Leu)	rs140389574	0.00009
NM_201550.4(LRRC10):c.348G>A (p.Glu116=)	rs778805482	0.00003
NM_001006630.2(CHRM2):c.186A>G (p.Leu62=)	rs760443842	0.00001
NM_201550.4(LRRC10):c.195T>C (p.Asn65=)	rs552658459	0.00001
NM_001006630.2(CHRM2):c.1107T>G (p.Thr369=)
NM_001006630.2(CHRM2):c.594A>G (p.Pro198=)	rs558678081

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