List of variants in gene DMD reported as benign by Center for Advanced Laboratory Medicine, UC San Diego Health, University of California San Diego

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: 9

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.1225A>T (p.Thr409Ser)	rs34155804	0.01079
NM_004006.3(DMD):c.2391T>G (p.Asn797Lys)	rs72468681	0.00714
NM_004006.3(DMD):c.1997C>T (p.Ser666Leu)	rs34563188	0.00460
NM_004006.3(DMD):c.9682T>C (p.Phe3228Leu)	rs141392048	0.00180
NM_004006.3(DMD):c.1513G>C (p.Val505Leu)	rs140340626	0.00113
NM_004006.3(DMD):c.4233+2C>T	rs147474070	0.00066
NM_004006.3(DMD):c.6320G>A (p.Arg2107Gln)	rs142807436	0.00036
NM_004006.3(DMD):c.2096C>G (p.Ala699Gly)	rs202008454	0.00018
NM_004006.3(DMD):c.5485C>G (p.Gln1829Glu)	rs754765424	0.00018

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.