List of variants in gene DMD reported as pathogenic for Abnormality of the musculature

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: 15

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.10141C>T (p.Arg3381Ter)	rs104894790
NM_004006.3(DMD):c.10171C>T (p.Arg3391Ter)	rs398123832
NM_004006.3(DMD):c.1083_1090del (p.Leu362fs)	rs2146833477
NM_004006.3(DMD):c.2032C>T (p.Gln678Ter)	rs398123872
NM_004006.3(DMD):c.2479G>T (p.Glu827Ter)	rs794727323
NM_004006.3(DMD):c.2584G>T (p.Glu862Ter)	rs2042975774
NM_004006.3(DMD):c.2698A>T (p.Lys900Ter)	rs2148583763
NM_004006.3(DMD):c.2804-1del	rs1557374667
NM_004006.3(DMD):c.2866C>T (p.Gln956Ter)	rs398123912
NM_004006.3(DMD):c.3314dup (p.Asn1106fs)	rs2148419527
NM_004006.3(DMD):c.5503C>T (p.Gln1835Ter)	rs1225638867
NM_004006.3(DMD):c.6576G>A (p.Trp2192Ter)	rs764789298
NM_004006.3(DMD):c.8601dup (p.Thr2868fs)	rs2149257286
NM_004006.3(DMD):c.9014T>A (p.Leu3005Ter)	rs2065150560
NM_004006.3(DMD):c.93+1G>A	rs886042604

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