List of variants in gene DMD reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized 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: 46

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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.7096A>C (p.Lys2366Gln)	rs1800275	0.21153
NM_004006.3(DMD):c.7728T>C (p.Asn2576=)	rs1801188	0.15883
NM_004006.3(DMD):c.837G>A (p.Thr279=)	rs1800265	0.12849
NM_004006.3(DMD):c.1635A>G (p.Arg545=)	rs5927083	0.12751
NM_004006.3(DMD):c.4234-13A>G	rs41303181	0.05327
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.6463C>T (p.Arg2155Trp)	rs1800273	0.02767
NM_004006.3(DMD):c.4162T>G (p.Phe1388Val)	rs28715870	0.02748
NM_004006.3(DMD):c.2623-11C>G	rs1028360	0.02567
NM_004006.3(DMD):c.-8T>A	rs113726961	0.02450
NM_004006.3(DMD):c.8762A>G (p.His2921Arg)	rs1800279	0.02191
NM_004006.3(DMD):c.4878G>T (p.Val1626=)	rs61733574	0.02120
NM_004006.3(DMD):c.5016T>A (p.Asn1672Lys)	rs16990264	0.02084
NM_004006.3(DMD):c.5724T>C (p.Asp1908=)	rs143159113	0.01630
NM_004006.3(DMD):c.3705C>T (p.Ala1235=)	rs143628111	0.01510
NM_004006.3(DMD):c.3021G>A (p.Ser1007=)	rs1800268	0.01212
NM_004006.3(DMD):c.1225A>T (p.Thr409Ser)	rs34155804	0.01079
NM_004006.3(DMD):c.3734C>T (p.Thr1245Ile)	rs1800269	0.01009
NM_004006.3(DMD):c.6322C>T (p.Arg2108Cys)	rs16990169	0.00981
NM_004006.3(DMD):c.*38G>A	rs16989352	0.00785
NM_004006.3(DMD):c.2391T>G (p.Asn797Lys)	rs72468681	0.00714
NM_004006.3(DMD):c.7476T>C (p.Val2492=)	rs142153424	0.00626
NM_004006.3(DMD):c.2143A>T (p.Thr715Ser)	rs16998350	0.00594
NM_004006.3(DMD):c.10789C>T (p.Leu3597=)	rs1800281	0.00486
NM_004006.3(DMD):c.1997C>T (p.Ser666Leu)	rs34563188	0.00460
NM_004006.3(DMD):c.1718C>T (p.Ala573Val)	rs5972599	0.00436
NM_004006.3(DMD):c.7542+13A>G	rs72466585	0.00407
NM_004006.3(DMD):c.3406A>T (p.Thr1136Ser)	rs3827462	0.00356
NM_004006.3(DMD):c.5182C>T (p.Arg1728Cys)	rs34102501	0.00327
NM_004006.3(DMD):c.802T>C (p.Leu268=)	rs1800264	0.00307
NM_004006.3(DMD):c.8218-798G>A	rs149479376	0.00299
NM_004006.3(DMD):c.2380+11G>A	rs183120304	0.00195
NM_004006.3(DMD):c.5265C>T (p.Pro1755=)	rs145515413	0.00124
NM_004006.3(DMD):c.3326A>T (p.Asn1109Ile)	rs200596739	0.00064
NM_004006.3(DMD):c.6828C>T (p.Pro2276=)	rs72466595	0.00039
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.4275A>G (p.Glu1425=)	rs72468647	0.00004
NM_004006.3(DMD):c.1869C>T (p.Leu623=)	rs1800267

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