List of variants in gene MYOD1 reported as pathogenic for hereditary skeletal muscle disorder

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_002478.5(MYOD1):c.188C>A (p.Ser63Ter)	rs147517396	0.00001
NM_002478.5(MYOD1):c.557dup (p.Arg188fs)	rs1179926739
NM_002478.5(MYOD1):c.697G>T (p.Glu233Ter)	rs768652299

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