List of variants in gene MYH11 reported as uncertain significance for Cardiovascular phenotype

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_002474.3(MYH11):c.217A>C (p.Lys73Gln)	rs147447269	0.00021
NM_002474.3(MYH11):c.3291C>T (p.Ala1097=)	rs147605116	0.00016
NM_002474.3(MYH11):c.1749+4C>G	rs776271431	0.00015
NM_002474.3(MYH11):c.3766A>C (p.Lys1256Gln)	rs149241435	0.00015
NM_002474.3(MYH11):c.3824G>T (p.Arg1275Leu)	rs267606901	0.00003
NM_002474.3(MYH11):c.2098C>T (p.Arg700Trp)	rs886038932	0.00001
NM_002474.3(MYH11):c.3619G>A (p.Glu1207Lys)	rs371831822	0.00001
NM_002474.3(MYH11):c.1115T>C (p.Met372Thr)	rs886038835
NM_002474.3(MYH11):c.1318G>A (p.Val440Met)	rs886038900
NM_002474.3(MYH11):c.2692G>A (p.Ala898Thr)	rs772769846
NM_002474.3(MYH11):c.3358A>G (p.Ile1120Val)	rs886038788
NM_002474.3(MYH11):c.3651+5_3651+11delinsG	rs371843272
NM_002474.3(MYH11):c.811G>A (p.Ala271Thr)	rs886038851

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