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

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Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_144573.4(NEXN):c.1174C>T (p.Arg392Ter)	rs750076188	0.00004
NM_001927.4(DES):c.1048C>T (p.Arg350Trp)	rs62636492	0.00002
NM_000257.4(MYH7):c.709C>T (p.Arg237Trp)	rs45516091	0.00001
NM_001267550.2(TTN):c.101107C>T (p.Arg33703Ter)	rs766265889	0.00001
NM_001267550.2(TTN):c.44364del (p.Tyr14789fs)	rs397517576
NM_001267550.2(TTN):c.52848del (p.Trp17616fs)
NM_001267550.2(TTN):c.60407_60410dup (p.Ile20138fs)
NM_001267550.2(TTN):c.65696_65706del (p.Lys21899fs)
NM_001267550.2(TTN):c.97647_97663dup (p.Thr32555delinsLysIleLysTyrLeuTer)	rs2154141588
NM_005572.4(LMNA):c.1711C>A (p.Arg571Ser)	rs80338938
NM_170707.4(LMNA):c.497G>C (p.Arg166Pro)	rs267607570

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