ClinVar Miner

List of variants in gene DMD reported by Stanford Center for Inherited Cardiovascular Disease,Stanford University

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 13
Download table as spreadsheet
NM_000109.4(DMD):c.1694del (p.Ala565fs) rs1569229528
NM_000109.4(DMD):c.1700T>C (p.Leu567Pro) rs370644567
NM_004006.2(DMD):c.10889G>A (p.Arg3630Gln) rs1057522606
NM_004006.2(DMD):c.3028G>C (p.Ala1010Pro) rs766325631
NM_004006.2(DMD):c.3971G>A (p.Arg1324His) rs768990357
NM_004006.2(DMD):c.4721G>A (p.Arg1574His) rs755206033
NM_004006.2(DMD):c.4951G>A (p.Asp1651Asn) rs1369953471
NM_004006.2(DMD):c.5530C>T (p.Arg1844Ter) rs1064325
NM_004006.2(DMD):c.7172A>G (p.Lys2391Arg) rs1556930538
NM_004006.2(DMD):c.7826G>A (p.Gly2609Asp) rs1060502649
NM_004006.2(DMD):c.8312A>C (p.Asp2771Ala) rs376720228
NM_004006.2(DMD):c.8983G>A (p.Val2995Ile) rs148643665
NM_004006.3(DMD):c.6571C>T (p.Arg2191Trp) rs149322279

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.