List of variants reported as uncertain significance for Primary dilated cardiomyopathy by Molecular Genetics, Royal Melbourne Hospital

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Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.586C>T (p.Arg196Cys)	rs369486891	0.00007
NM_014000.3(VCL):c.2531C>T (p.Pro844Leu)	rs145393322	0.00006
NM_001134363.3(RBM20):c.3578A>G (p.Tyr1193Cys)	rs535839168	0.00001
NM_001458.5(FLNC):c.1468C>T (p.Arg490Cys)	rs1422233407	0.00001
NM_001018005.2(TPM1):c.98A>C (p.Glu33Ala)	rs886039444
NM_001077653.2(TBX20):c.1003G>A (p.Gly335Arg)
NM_001134363.3(RBM20):c.122T>A (p.Met41Lys)
NM_001267550.2(TTN):c.58684A>G (p.Ile19562Val)	rs397517637
NM_001267550.2(TTN):c.9432C>T (p.Gly3144=)
NM_014000.3(VCL):c.1343T>C (p.Leu448Pro)
NM_015978.3(TNNI3K):c.92T>G (p.Leu31Ter)
NM_144573.4(NEXN):c.1112C>T (p.Pro371Leu)	rs200067011

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