List of variants in gene DMD reported as benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 15

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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.9649+15T>C	rs2293668	0.84201
NM_004006.3(DMD):c.2645A>G (p.Asp882Gly)	rs228406	0.69509
NM_004006.3(DMD):c.5234G>A (p.Arg1745His)	rs1801187	0.36912
NM_004006.3(DMD):c.8027+11C>T	rs2270672	0.33026
NM_004006.3(DMD):c.2168+13T>C	rs228373	0.32216
NM_004006.3(DMD):c.1635A>G (p.Arg545=)	rs5927083	0.12751
NM_004006.3(DMD):c.8734A>G (p.Asn2912Asp)	rs1800278	0.02976
NM_004006.3(DMD):c.8729A>T (p.Glu2910Val)	rs41305353	0.02876
NM_004006.3(DMD):c.4162T>G (p.Phe1388Val)	rs28715870	0.02748
NM_004006.3(DMD):c.4878G>T (p.Val1626=)	rs61733574	0.02120
NM_004006.3(DMD):c.5724T>C (p.Asp1908=)	rs143159113	0.01630
NM_004006.3(DMD):c.2391T>G (p.Asn797Lys)	rs72468681	0.00714
NM_004006.3(DMD):c.3432+10A>G	rs746260475	0.00010
NM_004006.3(DMD):c.3603+3dup	rs5902031

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