"Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3367169	NM_004006.3(DMD):c.9975-24G>A	DMD	Single nucleotide variant (intron variant)	Duchenne muscular dystrophy	GLikely benign
Select item 1799568	NM_004006.3(DMD):c.58A>C (p.Thr20Pro)	DMD (T12P +2 more)	Single nucleotide variant (missense variant +1 more)	Duchenne muscular dystrophy	GUncertain significance