ClinVar Miner

List of variants in gene DMD studied for Becker muscular dystrophy; Duchenne muscular dystrophy; Cardiomyopathy; Dystrophin deficiency

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
Download table as spreadsheet
NM_004006.2(DMD):c.1897A>T (p.Asn633Tyr) rs757047592
NM_004006.2(DMD):c.3379C>G (p.Leu1127Val) rs141887693
NM_004006.2(DMD):c.5076A>G (p.Thr1692=) rs145181319
NM_004006.2(DMD):c.960+9A>G rs886038537
NM_004006.2(DMD):c.9804A>G (p.Gln3268=) rs12690372
NM_004006.3(DMD):c.2645= (p.Asp882=) rs228406
NM_004006.3(DMD):c.265-438T>C rs1459975890
NM_004006.3(DMD):c.3510C>T (p.His1170=) rs138945423
NM_004006.3(DMD):c.5999A>T (p.Tyr2000Phe) rs1603630432
NM_004006.3(DMD):c.8027+11C>T rs2270672
NM_004006.3(DMD):c.8704C>T (p.Arg2902Trp) rs1188233243

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.