ClinVar Miner

List of variants in gene DMD reported as pathogenic by North West Genomic Laboratory Hub, Manchester University NHS Foundation Trust

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.1812+1G>A	rs373286166	0.00003
NM_004006.3(DMD):c.5794C>T (p.Gln1932Ter)	rs2097747388

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