List of variants in gene DMD reported as likely benign by Genetics and Genomics Program, Sidra Medicine

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.7571G>A (p.Arg2524His)	rs151244052	0.00109
NM_004006.3(DMD):c.5701G>A (p.Ala1901Thr)	rs201302282	0.00016
NM_004006.3(DMD):c.10228G>A (p.Val3410Ile)	rs751030250	0.00005
NM_004006.3(DMD):c.*39A>T	rs371730838	0.00001

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