List of variants in gene DMD reported as benign by Mendelics

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.8810G>A (p.Arg2937Gln)	rs1800280	0.95243
NM_004006.3(DMD):c.7096A>C (p.Lys2366Gln)	rs1800275	0.21153
NM_004006.3(DMD):c.9682T>C (p.Phe3228Leu)	rs141392048	0.00180
NM_004006.3(DMD):c.7183G>A (p.Ala2395Thr)	rs72466590	0.00126
NM_004006.3(DMD):c.7571G>A (p.Arg2524His)	rs151244052	0.00109
NM_004006.3(DMD):c.1318G>A (p.Glu440Lys)	rs189143447	0.00010
NM_004006.3(DMD):c.9564-536A>C	rs918777788

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