List of variants in gene MYH7 reported as pathogenic by Molecular Diagnostic Laboratory for Inherited Cardiovascular Disease, Montreal Heart Institute

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.1988G>A (p.Arg663His)	rs371898076	0.00004
NM_000257.4(MYH7):c.1357C>T (p.Arg453Cys)	rs121913625	0.00001
NM_000257.4(MYH7):c.1750G>A (p.Gly584Ser)	rs121913626	0.00001
NM_000257.4(MYH7):c.1816G>A (p.Val606Met)	rs121913627	0.00001
NM_000257.4(MYH7):c.2155C>T (p.Arg719Trp)	rs121913637	0.00001
NM_000257.4(MYH7):c.2722C>G (p.Leu908Val)	rs121913631	0.00001
NM_000257.4(MYH7):c.3578G>A (p.Arg1193His)	rs397516187	0.00001
NM_000257.4(MYH7):c.4130C>T (p.Thr1377Met)	rs397516201	0.00001
NM_000257.4(MYH7):c.428G>A (p.Arg143Gln)	rs397516209	0.00001
NM_000257.4(MYH7):c.727C>T (p.Arg243Cys)	rs397516265	0.00001
NM_000257.4(MYH7):c.1063G>A (p.Ala355Thr)	rs397516088
NM_000257.4(MYH7):c.1208G>A (p.Arg403Gln)	rs121913624
NM_000257.4(MYH7):c.1318G>A (p.Val440Met)	rs397516098
NM_000257.4(MYH7):c.1750G>C (p.Gly584Arg)	rs121913626
NM_000257.4(MYH7):c.2156G>A (p.Arg719Gln)	rs121913641
NM_000257.4(MYH7):c.2167C>G (p.Arg723Gly)	rs121913630
NM_000257.4(MYH7):c.2221G>T (p.Gly741Trp)	rs121913632
NM_000257.4(MYH7):c.2710C>T (p.Arg904Cys)	rs727503253
NM_000257.4(MYH7):c.2711G>A (p.Arg904His)	rs397516165
NM_000257.4(MYH7):c.611G>T (p.Arg204Leu)	rs397516260
NM_000257.4(MYH7):c.732+1G>A	rs730880850
NM_000257.4(MYH7):c.746G>A (p.Arg249Gln)	rs3218713
NM_000257.4(MYH7):c.788T>C (p.Ile263Thr)	rs397516269

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