List of variants in gene combination MYH2, MYHAS reported as benign by Invitae

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_017534.6(MYH2):c.324A>G (p.Glu108=)	rs12600539	0.42634
NM_017534.6(MYH2):c.904+10G>A	rs719277	0.39768
NM_017534.6(MYH2):c.3263+15A>G	rs2277651	0.34231
NM_017534.6(MYH2):c.1975-9G>A	rs3744566	0.06015
NM_017534.6(MYH2):c.5674-10T>C	rs16943488	0.01300
NM_017534.6(MYH2):c.2967A>G (p.Ala989=)	rs113190032	0.01110
NM_017534.6(MYH2):c.183G>A (p.Thr61=)	rs142539913	0.00745
NM_017534.6(MYH2):c.2382C>A (p.Thr794=)	rs76400103	0.00548
NM_017534.6(MYH2):c.4242C>T (p.Asn1414=)	rs146615128	0.00548
NM_017534.6(MYH2):c.4329C>T (p.Ala1443=)	rs61739663	0.00465
NM_017534.6(MYH2):c.5780G>A (p.Arg1927Gln)	rs34161789	0.00444
NM_017534.6(MYH2):c.2295G>A (p.Gly765=)	rs79757188	0.00317
NM_017534.6(MYH2):c.2698-8A>C	rs186620412	0.00221
NM_017534.6(MYH2):c.2106C>T (p.Asn702=)	rs145039915	0.00085
NM_017534.6(MYH2):c.3585G>A (p.Ala1195=)	rs143988052	0.00068
NM_017534.6(MYH2):c.2062+8A>G	rs117562194	0.00039
NM_017534.6(MYH2):c.2304+7T>G	rs370223713	0.00034
NM_017534.6(MYH2):c.2414T>C (p.Val805Ala)	rs200662973	0.00034
NM_017534.6(MYH2):c.2889T>C (p.Leu963=)	rs146355976	0.00031
NM_017534.6(MYH2):c.3128C>T (p.Ser1043Phe)	rs200217946	0.00026
NM_017534.6(MYH2):c.4258C>T (p.Leu1420Phe)	rs187438258	0.00019
NM_017534.6(MYH2):c.1161G>A (p.Ala387=)	rs141134519	0.00006
NM_017534.6(MYH2):c.1068G>C (p.Thr356=)	rs116419997
NM_017534.6(MYH2):c.1975-14dup
NM_017534.6(MYH2):c.1975-9G>C	rs3744566
NM_017534.6(MYH2):c.399T>A (p.Pro133=)	rs11078850
NM_017534.6(MYH2):c.4007C>A (p.Ala1336Glu)	rs138470281

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