List of variants in gene MYH7 reported as benign by Genetic Services Laboratory, University of Chicago

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_000257.4(MYH7):c.189C>T (p.Thr63=)	rs2069540	0.51373
NM_000257.4(MYH7):c.2967T>C (p.Ile989=)	rs7157716	0.43030
NM_000257.4(MYH7):c.732C>T (p.Phe244=)	rs2069542	0.26492
NM_000257.4(MYH7):c.1128C>T (p.Asp376=)	rs2231126	0.15761
NM_000257.4(MYH7):c.1095G>A (p.Lys365=)	rs735711	0.13321
NM_000257.4(MYH7):c.1605A>G (p.Glu535=)	rs2069543	0.03103
NM_000257.4(MYH7):c.597A>G (p.Ala199=)	rs2069541	0.00877
NM_000257.4(MYH7):c.3337-4dup	rs45504498

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