List of variants in gene DMD reported as pathogenic by Broad Center for Mendelian Genomics, Broad Institute of MIT and Harvard

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
GRCh38/hg38 Xp21.1(chrX:31601428-31727780)x0
NM_004006.3(DMD):c.5407C>T (p.Gln1803Ter)	rs1557294228
NM_004006.3(DMD):c.5697del (p.Lys1899fs)	rs794727661
NM_004006.3(DMD):c.7159C>T (p.Gln2387Ter)	rs1556930579

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