ClinVar Miner

List of variants in gene DMD reported as likely pathogenic by Juno Genomics, Hangzhou Juno Genomics, Inc

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.8277_8278insT (p.Gln2760fs)
NM_004006.3(DMD):c.9336_9344del (p.Arg3113_Leu3115del)
NM_004006.3(DMD):c.9563+1215A>G

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