List of variants in gene DMD reported as pathogenic by Genomic Center, National Cancer Institute

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.1713del (p.Phe571fs)	rs1601808932
NM_004006.3(DMD):c.2920del (p.Ile974fs)	rs2040714896
NM_004006.3(DMD):c.4072-267del	rs753288164

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