C0013264[trait identifier] AND "Institute of Medical Genetics and Appl - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 94500	NM_004006.3(DMD):c.2281_2285del (p.Glu761fs)	DMD (E638fs +3 more)	Deletion (frameshift variant)	not provided +1 more	GPathogenic
Select item 2664331	NM_004006.3(DMD):c.489G>A (p.Trp163Ter)	DMD (W163* +3 more)	Single nucleotide variant (nonsense)	Duchenne muscular dystrophy	GPathogenic
Select item 29962	NM_004006.3(DMD):c.9G>A (p.Trp3Ter)	DMD (W3*)	Single nucleotide variant (nonsense +1 more)	not provided +3 more	GPathogenic

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