List of variants reported as benign for dilated cardiomyopathy 1D by Genome-Nilou Lab

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Total variants: 26

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.163+120T>C	rs3729842	0.84150
NM_001276345.2(TNNT2):c.601-32A>C	rs1104859	0.73965
NM_001276345.2(TNNT2):c.348C>T (p.Ile116=)	rs3729547	0.69444
NM_001276345.2(TNNT2):c.811-122C>G	rs45509695	0.22049
NM_001276345.2(TNNT2):c.811-33C>T	rs2275863	0.22049
NM_001276345.2(TNNT2):c.610-90G>A	rs11810834	0.03251
NM_001276345.2(TNNT2):c.*66G>A	rs3729998	0.01883
NM_001276345.2(TNNT2):c.163+12G>A	rs45580032	0.01441
NM_001276345.2(TNNT2):c.42-20G>A	rs45561443	0.01192
NM_001276345.2(TNNT2):c.294+7G>A	rs45490292	0.01066
NM_001276345.2(TNNT2):c.68-8A>G	rs115805892	0.00864
NM_001276345.2(TNNT2):c.610-81C>T	rs28730745	0.00831
NM_001276345.2(TNNT2):c.200-29C>G	rs45449197	0.00690
NM_001276345.2(TNNT2):c.53-47C>G	rs45553832	0.00345
NM_001276345.2(TNNT2):c.68-5C>T	rs540630390	0.00133
NM_001276345.2(TNNT2):c.98-81G>A	rs45576939	0.00067
NM_001276345.2(TNNT2):c.295-19C>T	rs587780969	0.00009
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=)	rs200283086	0.00006
NM_001276345.2(TNNT2):c.295-14C>T	rs747477576	0.00006
NM_001276345.2(TNNT2):c.52+13G>A	rs376820377	0.00004
NM_001276345.2(TNNT2):c.164-50G>A	rs3729843
NM_001276345.2(TNNT2):c.270C>T (p.Pro90=)	rs140245123
NM_001276345.2(TNNT2):c.351G>A (p.Glu117=)	rs1659436211
NM_001276345.2(TNNT2):c.412-6_412-4del	rs397516462
NM_001276345.2(TNNT2):c.412-94del	rs35559054
NM_001276345.2(TNNT2):c.53-11_53-7del	rs45533739

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