List of variants in gene MYH7 reported as likely benign 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.1002C>T (p.Asn334=)	rs34803781	0.01418
NM_000257.4(MYH7):c.4239G>A (p.Ser1413=)	rs3729821	0.00267
NM_000257.4(MYH7):c.2945T>C (p.Met982Thr)	rs145532615	0.00095
NM_000257.4(MYH7):c.2890G>C (p.Val964Leu)	rs45496496	0.00050
NM_000257.4(MYH7):c.77C>T (p.Ala26Val)	rs186964570	0.00021
NM_000257.4(MYH7):c.3564T>C (p.Thr1188=)	rs45587932	0.00009
NM_000257.4(MYH7):c.1000-7C>T	rs200129563	0.00006
NM_000257.4(MYH7):c.5704G>C (p.Glu1902Gln)	rs187073962	0.00002
NM_000257.4(MYH7):c.2727C>A (p.Ile909=)	rs377722048	0.00001
NM_000257.4(MYH7):c.3235C>T (p.Arg1079Trp)	rs192722540	0.00001

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