List of variants in gene MYH7 reported as benign by Ambry Genetics

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: 20

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.189C>T (p.Thr63=)	rs2069540	0.51584
NM_000257.4(MYH7):c.2967T>C (p.Ile989=)	rs7157716	0.43030
NM_000257.4(MYH7):c.732C>T (p.Phe244=)	rs2069542	0.27385
NM_000257.4(MYH7):c.1128C>T (p.Asp376=)	rs2231126	0.15761
NM_000257.4(MYH7):c.1095G>A (p.Lys365=)	rs735711	0.13859
NM_000257.4(MYH7):c.1062C>T (p.Gly354=)	rs735712	0.06133
NM_000257.4(MYH7):c.1605A>G (p.Glu535=)	rs2069543	0.03319
NM_000257.4(MYH7):c.895+17G>A	rs45580436	0.02377
NM_000257.4(MYH7):c.975C>T (p.Asp325=)	rs2231124	0.01865
NM_000257.4(MYH7):c.1002C>T (p.Asn334=)	rs34803781	0.01418
NM_000257.4(MYH7):c.1767C>T (p.Asn589=)	rs3729816	0.01311
NM_000257.4(MYH7):c.3972+15C>T	rs3729820	0.01159
NM_000257.4(MYH7):c.597A>G (p.Ala199=)	rs2069541	0.00853
NM_000257.4(MYH7):c.3153G>A (p.Ala1051=)	rs45540831	0.00505
NM_000257.4(MYH7):c.1579-17C>T	rs182949516	0.00470
NM_000257.4(MYH7):c.4239G>A (p.Ser1413=)	rs3729821	0.00267
NM_000257.4(MYH7):c.3351G>A (p.Glu1117=)	rs45554236	0.00217
NM_000257.4(MYH7):c.3690C>T (p.Asp1230=)	rs370750044	0.00038
NM_000257.4(MYH7):c.3337-4dup	rs45504498
NM_000257.4(MYH7):c.3770A>G (p.Asn1257Ser)	rs574005462

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