List of variants reported as not provided for Dilated cardiomyopathy 1G; Autosomal recessive limb-girdle muscular dystrophy type 2J; Tibial muscular dystrophy; Myopathy, myofibrillar, 9, with early respiratory failure; Early-onset myopathy with fatal cardiomyopathy; Hypertrophic cardiomyopathy 9

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_001267550.2(TTN):c.24820G>A (p.Glu8274Lys)	rs72648981	0.00245
NM_001267550.2(TTN):c.68458G>C (p.Ala22820Pro)	rs72646880	0.00151
NM_133379.5(TTN):c.11075G>C (p.Ser3692Thr)	rs147314430	0.00071
NM_001267550.2(TTN):c.9610C>T (p.Arg3204Ter)	rs757836789	0.00003
NM_001267550.2(TTN):c.23879G>A (p.Ser7960Asn)	rs369302142	0.00001
NM_001267550.2(TTN):c.69051A>G (p.Glu23017=)	rs770296752
NM_001267550.2(TTN):c.72390G>C (p.Leu24130Phe)	rs376664950

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