List of variants in gene combination MYH8, MYHAS reported as benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002472.3(MYH8):c.714T>C (p.Thr238=)	rs8068729	0.86861
NM_002472.3(MYH8):c.5074T>C (p.Trp1692Arg)	rs8069834	0.50046
NM_002472.3(MYH8):c.5208C>T (p.Asp1736=)	rs33969260	0.17467

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