List of variants in gene MYH7 reported as pathogenic for dilated cardiomyopathy 1S

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: 34

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.1988G>A (p.Arg663His)	rs371898076	0.00005
NM_000257.4(MYH7):c.2081G>A (p.Arg694His)	rs886039030	0.00003
NM_000257.4(MYH7):c.611G>A (p.Arg204His)	rs397516260	0.00003
NM_000257.4(MYH7):c.2167C>T (p.Arg723Cys)	rs121913630	0.00002
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.2681A>G (p.Glu894Gly)	rs397516161	0.00001
NM_000257.4(MYH7):c.2717A>G (p.Asp906Gly)	rs267606908	0.00001
NM_000257.4(MYH7):c.4258C>T (p.Arg1420Trp)	rs145213771	0.00001
NM_000257.4(MYH7):c.5655G>A (p.Ala1885=)	rs753392652	0.00001
NM_000257.4(MYH7):c.728G>A (p.Arg243His)	rs267606910	0.00001
NM_000257.4(MYH7):c.1207C>T (p.Arg403Trp)	rs3218714
NM_000257.4(MYH7):c.1208G>A (p.Arg403Gln)	rs121913624
NM_000257.4(MYH7):c.1573G>A (p.Glu525Lys)	rs606231324
NM_000257.4(MYH7):c.1594T>C (p.Ser532Pro)	rs121913642
NM_000257.4(MYH7):c.1925C>T (p.Ser642Leu)	rs121913646
NM_000257.4(MYH7):c.1963C>A (p.Leu655Met)	rs1595084583
NM_000257.4(MYH7):c.1987C>T (p.Arg663Cys)	rs397516127
NM_000257.4(MYH7):c.2163-1G>A	rs606231334
NM_000257.4(MYH7):c.2207T>C (p.Ile736Thr)	rs727503261
NM_000257.4(MYH7):c.2221G>C (p.Gly741Arg)	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.2770G>A (p.Glu924Lys)	rs121913628
NM_000257.4(MYH7):c.2788G>C (p.Glu930Gln)	rs397516171
NM_000257.4(MYH7):c.5378T>C (p.Leu1793Pro)	rs121913654
NM_000257.4(MYH7):c.5378_5380del (p.Leu1793del)	rs587779396
NM_000257.4(MYH7):c.5740G>A (p.Glu1914Lys)	rs397516254
NM_000257.4(MYH7):c.5754C>R (p.Asn1918Lys)	rs138110910
NM_000257.4(MYH7):c.602T>C (p.Ile201Thr)	rs397516258
NM_000257.4(MYH7):c.667G>A (p.Ala223Thr)	rs121913645
NM_000257.4(MYH7):c.732+1G>A	rs730880850
NM_000257.4(MYH7):c.746G>A (p.Arg249Gln)	rs3218713
NM_000257.4(MYH7):c.847T>G (p.Tyr283Asp)	rs397515482

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