ClinVar Miner

List of variants in gene DMD reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
Download table as spreadsheet
HGVS dbSNP
NM_004006.2(DMD):c.1047A>T (p.Glu349Asp) rs1044325754
NM_004006.2(DMD):c.1310C>G (p.Ala437Gly) rs1556875180
NM_004006.2(DMD):c.1331+2dup rs1556875106
NM_004006.2(DMD):c.139G>T (p.Gly47Trp) rs1557084183
NM_004006.2(DMD):c.2176G>T (p.Val726Phe) rs886044365
NM_004006.2(DMD):c.3239A>G (p.Asp1080Gly) rs886043493
NM_004006.2(DMD):c.419T>G (p.Leu140Arg) rs1557052675
NM_004006.2(DMD):c.4409G>A (p.Arg1470His)
NM_004006.2(DMD):c.5518G>C (p.Asp1840His) rs905571950
NM_004006.2(DMD):c.6196G>T (p.Ala2066Ser)
NM_004006.2(DMD):c.6290+5G>A rs886043467
NM_004006.2(DMD):c.6762G>C (p.Lys2254Asn)
NM_004006.2(DMD):c.711A>C (p.Gln237His) rs778632674
NM_004006.2(DMD):c.7201-4A>G rs1556917126
NM_004006.2(DMD):c.7919C>G (p.Ala2640Gly) rs146020545
NM_004006.2(DMD):c.8138A>G (p.Asn2713Ser) rs758633794

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.