"Phosphorus, Inc."[submitter] AND "DMD"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 11268	NM_004006.3(DMD):c.8734A>G (p.Asn2912Asp)	DMD (N2912D +7 more)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign
Select item 11267	NM_004006.3(DMD):c.8729A>T (p.Glu2910Val)	DMD (E2910V +7 more)	Single nucleotide variant (missense variant)	Duchenne muscular dystrophy +4 more	GBenign/Likely benign
Select item 94776	NM_004006.3(DMD):c.7728T>C (p.Asn2576=)	DMD	Single nucleotide variant (synonymous variant)	not specified +5 more	GBenign
Select item 94657	NM_004006.3(DMD):c.5234G>A (p.Arg1745His)	DMD (R1745H +5 more)	Single nucleotide variant (missense variant)	Cardiovascular phenotype +4 more	GBenign
Select item 94476	NM_004006.3(DMD):c.1635A>G (p.Arg545=)	DMD	Single nucleotide variant (synonymous variant)	not provided +5 more	GBenign
Select item 94844	NM_004006.3(DMD):c.94-9dup	DMD	Duplication (intron variant)	Dilated cardiomyopathy 3B +4 more	GBenign/Likely benign

ClinVar