List of variants reported as likely benign for Dilated cardiomyopathy 1S by Illumina Laboratory Services, Illumina

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Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.1002C>T (p.Asn334=)	rs34803781	0.01316
NM_000257.4(MYH7):c.4472C>G (p.Ser1491Cys)	rs3729823	0.00861
NM_000257.4(MYH7):c.4239G>A (p.Ser1413=)	rs3729821	0.00267
NM_000257.4(MYH7):c.2945T>C (p.Met982Thr)	rs145532615	0.00093
NM_000257.4(MYH7):c.2890G>C (p.Val964Leu)	rs45496496	0.00050
NM_000257.4(MYH7):c.2349C>T (p.Arg783=)	rs139882431	0.00036
NM_000257.4(MYH7):c.77C>T (p.Ala26Val)	rs186964570	0.00031
NM_000257.4(MYH7):c.3564T>C (p.Thr1188=)	rs45587932	0.00016
NM_000257.4(MYH7):c.2359C>T (p.Arg787Cys)	rs145677314	0.00009
NM_000257.4(MYH7):c.2360G>A (p.Arg787His)	rs376754645	0.00008
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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