List of variants in gene DMD reported as likely pathogenic for Becker muscular dystrophy; Duchenne muscular dystrophy; Dilated cardiomyopathy 3B

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.6763-2A>G	rs398124033	0.00001
NM_004006.3(DMD):c.10509del (p.Glu3505fs)
NM_004006.3(DMD):c.1375G>T (p.Glu459Ter)	rs2149350253
NM_004006.3(DMD):c.2292+1G>T
NM_004006.3(DMD):c.4846-1G>C	rs1603631757
NM_004006.3(DMD):c.6614+3310G>T	rs797045526
NM_004006.3(DMD):c.8277_8278insT (p.Gln2760fs)
NM_004006.3(DMD):c.832-1G>T
NM_004006.3(DMD):c.9336_9344del (p.Arg3113_Leu3115del)
NM_004006.3(DMD):c.960+2T>G	rs776457078

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