List of variants in gene DMD reported as benign by Genome-Nilou Lab

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.1993-37T>G	rs115571	0.71699
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.6614+26G>T	rs3761604	0.28231
NM_004006.3(DMD):c.7096A>C (p.Lys2366Gln)	rs1800275	0.21153
NM_004006.3(DMD):c.7728T>C (p.Asn2576=)	rs1801188	0.15883
NM_004006.3(DMD):c.6290+27T>A	rs3788896	0.12062
NM_004006.3(DMD):c.4234-13A>G	rs41303181	0.05327
NM_004006.3(DMD):c.5181A>T (p.Ile1727=)	rs200887855	0.00038
NM_004006.3(DMD):c.1095A>C (p.Gln365His)	rs1800266	0.00035
NM_004006.3(DMD):c.1713T>A (p.Phe571Leu)	rs587782936	0.00005

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