C4016477[trait identifier] AND "OMIM"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 94430	NM_004006.3(DMD):c.10223+1G>A	DMD	Single nucleotide variant (splice donor variant +1 more)	not provided +2 more	GPathogenic
Select item 11246	NM_004006.3(DMD):c.1438G>T (p.Gly480Ter)	DMD (G480* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy	GPathogenic
Select item 11238	NM_004006.3(DMD):c.174_175del (p.Gly59fs)	DMD (G51fs +2 more)	Deletion (frameshift variant +1 more)	Intermediate muscular dystrophy	GPathogenic

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