List of variants in gene DMD reported as pathogenic for 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.1724T>C (p.Leu575Pro)	rs370644567	0.00006
NM_004006.2(DMD):c.(?_32)_(649_?)del
NM_004006.3(DMD):c.1150-14_1158dup	rs2519636860
NM_004006.3(DMD):c.4271T>A (p.Leu1424Ter)	rs2097991272

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