ClinVar Miner

List of variants reported as likely pathogenic for Duchenne muscular dystrophy by Centro de Genética y Biología Molecular, Universidad de San Martín de Porres

Included ClinVar conditions (4):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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.1672del (p.Leu558fs)	rs2052703269
NM_004006.3(DMD):c.6253del (p.Trp2085fs)	rs2097447453
NM_004006.3(DMD):c.803del (p.Leu268fs)	rs2063891560

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