List of variants in gene MYH11 reported as likely benign by Genome Diagnostics Laboratory, Amsterdam University Medical Center

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_002474.3(MYH11):c.2520+17A>G	rs185697714	0.00383
NM_002474.3(MYH11):c.3828G>A (p.Ala1276=)	rs113154524	0.00240
NM_002474.3(MYH11):c.3652-6C>T	rs193922630	0.00219
NM_002474.3(MYH11):c.739C>T (p.Arg247Cys)	rs150759461	0.00174
NM_002474.3(MYH11):c.3102T>C (p.Ser1034=)	rs181744522	0.00080
NM_002474.3(MYH11):c.2005C>T (p.Arg669Cys)	rs111404182	0.00079
NM_002474.3(MYH11):c.2049C>T (p.His683=)	rs150924100	0.00061
NM_002474.3(MYH11):c.12G>A (p.Lys4=)	rs112650390	0.00057
NM_002474.3(MYH11):c.3031T>C (p.Leu1011=)	rs112861184	0.00053
NM_002474.3(MYH11):c.2893G>T (p.Ala965Ser)	rs113696032	0.00031
NM_002474.3(MYH11):c.914A>G (p.Asn305Ser)	rs185661462	0.00026
NM_002474.3(MYH11):c.2802G>A (p.Glu934=)	rs138977949	0.00024
NM_002474.3(MYH11):c.3858+16G>C	rs370164910	0.00013
NM_002474.3(MYH11):c.633+1900G>A	rs371799677	0.00013
NM_002474.3(MYH11):c.690C>T (p.Asn230=)	rs561105158	0.00009
NM_002474.3(MYH11):c.300C>T (p.Ser100=)	rs111662326	0.00008
NM_002474.3(MYH11):c.1575+7G>A	rs754750176	0.00004
NM_002474.3(MYH11):c.1440C>T (p.Asn480=)	rs554373758	0.00003
NM_002474.3(MYH11):c.1413C>T (p.Phe471=)	rs758885290	0.00002
NM_002474.3(MYH11):c.3294-10del	rs756946356	0.00001
NM_002474.3(MYH11):c.1569G>A (p.Glu523=)	rs1555562769
NM_002474.3(MYH11):c.2998-18_2998-17del	rs746744616
NM_002474.3(MYH11):c.530+20C>T	rs780914854

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