C4551827[trait identifier] AND "Molecular Genetics, Royal Melbourne Ho - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1052902	NM_004006.3(DMD):c.7993A>G (p.Asn2665Asp)	DMD (N1321D +6 more)	Single nucleotide variant (missense variant)	Progressive muscular dystrophy +1 more	GUncertain significance
Select item 1355209	NM_004006.3(DMD):c.2365G>A (p.Glu789Lys)	DMD (E666K +3 more)	Single nucleotide variant (missense variant)	Progressive muscular dystrophy +2 more	GConflicting classifications of pathogenicity