List of variants in gene DMD reported as likely pathogenic for not specified

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
GRCh37/hg19 Xp21.1(chrX:31761311-31858935)
GRCh37/hg19 Xp21.1(chrX:31776812-31899686)
GRCh37/hg19 Xp21.1(chrX:31881035-31993637)
NM_004006.3(DMD):c.5922+4A>G	rs1603631218

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