"MYOD1-related disorder"[Disease/phenotype] AND "PreventionGenetics, p - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3049014	NM_002478.5(MYOD1):c.78G>A (p.Thr26=)	MYOD1	Single nucleotide variant (synonymous variant)	MYOD1-related disorder	GLikely benign
Select item 788828	NM_002478.5(MYOD1):c.219G>A (p.Pro73=)	MYOD1	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 3057336	NM_002478.5(MYOD1):c.225A>C (p.Ala75=)	MYOD1	Single nucleotide variant (synonymous variant)	MYOD1-related disorder	GLikely benign
Select item 3055802	NM_002478.5(MYOD1):c.630+9G>T	MYOD1	Single nucleotide variant (intron variant)	MYOD1-related disorder	GBenign
Select item 730409	NM_002478.5(MYOD1):c.710-4G>C	MYOD1	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 731111	NM_002478.5(MYOD1):c.768G>A (p.Val256=)	MYOD1	Single nucleotide variant (synonymous variant)	MYOD1-related disorder +1 more	GBenign/Likely benign
Select item 3039547	NM_002478.5(MYOD1):c.878G>A (p.Ser293Asn)	MYOD1 (S293N)	Single nucleotide variant (missense variant)	MYOD1-related disorder	GBenign
Select item 711460	NM_002478.5(MYOD1):c.915G>A (p.Pro305=)	MYOD1	Single nucleotide variant (synonymous variant)	MYOD1-related disorder +1 more	GLikely benign

ClinVar