ClinVar Miner

List of variants in gene DMD reported as likely pathogenic by Genomic Medicine Center of Excellence, King Faisal Specialist Hospital and Research Centre

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.2168+1G>T	rs1057518207
NM_004006.3(DMD):c.3922-3C>T	rs786205603
NM_004006.3(DMD):c.4444A>T (p.Lys1482Ter)

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