List of variants reported as uncertain significance for Dilated cardiomyopathy 1S by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.4031G>A (p.Arg1344Gln)	rs797045097	0.00002
NM_000257.4(MYH7):c.5020G>A (p.Val1674Met)	rs397516235	0.00002
NM_000257.4(MYH7):c.5096G>A (p.Arg1699Gln)	rs146778113	0.00002
NM_000257.4(MYH7):c.1633G>A (p.Asp545Asn)	rs564101364	0.00001
NM_000257.4(MYH7):c.3778C>T (p.Arg1260Trp)	rs755386220	0.00001
NM_000257.4(MYH7):c.4717G>A (p.Glu1573Lys)	rs750987717	0.00001
NM_000257.4(MYH7):c.5639G>A (p.Arg1880His)	rs867477685	0.00001
NM_000257.4(MYH7):c.5726G>A (p.Arg1909Gln)	rs397516253	0.00001
NM_000257.4(MYH7):c.1105C>T (p.Arg369Trp)	rs1318155896
NM_000257.4(MYH7):c.1407T>G (p.Asp469Glu)
NM_000257.4(MYH7):c.2581G>A (p.Glu861Lys)	rs868789318
NM_000257.4(MYH7):c.3577C>T (p.Arg1193Cys)	rs886039090
NM_000257.4(MYH7):c.3994G>C (p.Ala1332Pro)
NM_000257.4(MYH7):c.5410G>A (p.Ala1804Thr)	rs730880818

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