List of variants in gene DMD reported as benign by PreventionGenetics, part of Exact Sciences

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.9649+15T>C	rs2293668	0.84201
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.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.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.3705C>T (p.Ala1235=)	rs143628111	0.01510
NM_004006.3(DMD):c.4344+17A>T	rs72468646	0.01496
NM_004006.3(DMD):c.3021G>A (p.Ser1007=)	rs1800268	0.01212
NM_004006.3(DMD):c.1554T>A (p.Asp518Glu)	rs61733587	0.01098
NM_004006.3(DMD):c.1225A>T (p.Thr409Ser)	rs34155804	0.01079
NM_004006.3(DMD):c.31+36949C>T	rs182597890	0.01020
NM_004006.3(DMD):c.3734C>T (p.Thr1245Ile)	rs1800269	0.01009
NM_004006.3(DMD):c.7476T>C (p.Val2492=)	rs142153424	0.00626
NM_004006.3(DMD):c.3432+2036A>C	rs182575709	0.00580
NM_004006.3(DMD):c.7542+13A>G	rs72466585	0.00407
NM_004006.3(DMD):c.5182C>T (p.Arg1728Cys)	rs34102501	0.00327
NM_004006.3(DMD):c.9682T>C (p.Phe3228Leu)	rs141392048	0.00180
NM_004006.3(DMD):c.9225-5795G>A	rs138287985	0.00025
NM_004006.3(DMD):c.5163G>C (p.Lys1721Asn)	rs72468630	0.00021
NM_004006.3(DMD):c.3567T>A (p.Thr1189=)	rs370685748	0.00001
NM_004006.3(DMD):c.6140A>G (p.Gln2047Arg)	rs773782786	0.00001
NM_004006.3(DMD):c.1869C>T (p.Leu623=)	rs1800267
NM_004006.3(DMD):c.2569C>T (p.Pro857Ser)	rs552275776
NM_004006.3(DMD):c.94-9dup	rs3834997

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