List of variants in gene DMD reported as likely 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: 38

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HGVS	dbSNP	gnomAD frequency
NM_004006.3(DMD):c.6463C>T (p.Arg2155Trp)	rs1800273	0.02767
NM_004006.3(DMD):c.2623-11C>G	rs1028360	0.02567
NM_004006.3(DMD):c.8762A>G (p.His2921Arg)	rs1800279	0.02191
NM_004006.3(DMD):c.832-17C>A	rs72470514	0.01678
NM_004006.3(DMD):c.832-18C>G	rs72470515	0.01505
NM_004006.3(DMD):c.3021G>A (p.Ser1007=)	rs1800268	0.01212
NM_004006.3(DMD):c.3734C>T (p.Thr1245Ile)	rs1800269	0.01009
NM_004006.3(DMD):c.3603+8A>G	rs193249735	0.00743
NM_004006.3(DMD):c.3787-18T>C	rs72468656	0.00621
NM_004006.3(DMD):c.10789C>T (p.Leu3597=)	rs1800281	0.00486
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.3970C>T (p.Arg1324Cys)	rs143184877	0.00208
NM_004006.3(DMD):c.1483-7C>G	rs112463388	0.00162
NM_004006.3(DMD):c.8571T>C (p.Thr2857=)	rs72466570	0.00153
NM_004006.3(DMD):c.2971G>C (p.Glu991Gln)	rs72468667	0.00146
NM_004006.3(DMD):c.7571G>A (p.Arg2524His)	rs151244052	0.00109
NM_004006.3(DMD):c.4233+2C>T	rs147474070	0.00066
NM_004006.3(DMD):c.2457A>C (p.Leu819=)	rs72468680	0.00046
NM_004006.3(DMD):c.2490C>T (p.Asn830=)	rs72468679	0.00040
NM_004006.3(DMD):c.6828C>T (p.Pro2276=)	rs72466595	0.00039
NM_004006.3(DMD):c.1934A>G (p.Asp645Gly)	rs147822019	0.00036
NM_004006.3(DMD):c.3163-18T>C	rs72468662	0.00036
NM_004006.3(DMD):c.5010G>T (p.Trp1670Cys)	rs727503828	0.00032
NM_004006.3(DMD):c.2386G>A (p.Val796Ile)	rs139726281	0.00023
NM_004006.3(DMD):c.7310-7A>G	rs373230021	0.00023
NM_004006.3(DMD):c.6571C>T (p.Arg2191Trp)	rs149322279	0.00020
NM_004006.3(DMD):c.9486G>A (p.Glu3162=)	rs370724251	0.00015
NM_004006.3(DMD):c.8027+7A>T	rs72466580	0.00013
NM_004006.3(DMD):c.8027+13T>G	rs772027445	0.00009
NM_004006.3(DMD):c.4275A>G (p.Glu1425=)	rs72468647	0.00004
NM_004006.3(DMD):c.6614+7C>T	rs180719577	0.00003
NM_004006.3(DMD):c.6072T>C (p.Cys2024=)	rs373804251	0.00002
NM_004006.3(DMD):c.9291C>T (p.Asp3097=)	rs796934165	0.00001
NM_004006.3(DMD):c.23_35del	rs752332058
NM_004006.3(DMD):c.2168+11C>G	rs376214348
NM_004006.3(DMD):c.3603+3_3603+4dup	rs5902031
NM_004006.3(DMD):c.923C>T (p.Thr308Ile)	rs145064612

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