List of variants in gene DMD reported as pathogenic for Becker muscular dystrophy; Duchenne muscular dystrophy

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.10454del (p.Leu3485fs)	rs398123839
NM_004006.3(DMD):c.1510C>T (p.Gln504Ter)	rs2149265022
NM_004006.3(DMD):c.3256A>T (p.Lys1086Ter)	rs745585519
NM_004006.3(DMD):c.5794C>T (p.Gln1932Ter)	rs2097747388
Single allele

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