List of variants in gene DMD reported as pathogenic by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.1812+1G>A	rs373286166	0.00003
NM_004006.2(DMD):c.10453dup (p.Leu3485Profs)	rs886043375
NM_004006.3(DMD):c.10098AGA[1] (p.Glu3367del)	rs886042840
NM_004006.3(DMD):c.10108C>T (p.Arg3370Ter)	rs104894787
NM_004006.3(DMD):c.2669T>A (p.Leu890Ter)	rs1557380616
NM_004006.3(DMD):c.31+1G>T	rs398123923
NM_004006.3(DMD):c.3295C>T (p.Gln1099Ter)	rs398123935
NM_004006.3(DMD):c.5324_5325delinsGT (p.Lys1775Ser)	rs1557303381
NM_004006.3(DMD):c.630del (p.Lys211fs)	rs1557047827
NM_004006.3(DMD):c.6502G>T (p.Glu2168Ter)	rs779739455
NM_004006.3(DMD):c.7310-1G>A	rs1556880354
NM_004006.3(DMD):c.9854_9863del (p.Met3285fs)	rs398124105

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