ClinVar Miner

List of variants in gene DMD reported as benign by GeneDx

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Gene type:
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Total variants: 82
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HGVS dbSNP
NM_000109.3(DMD):c.9658T>C (p.Phe3220Leu) rs141392048
NM_004006.2(DMD):c.-72562A>G rs113880711
NM_004006.2(DMD):c.-72567T>C rs587780921
NM_004006.2(DMD):c.-72599T>C rs587780920
NM_004006.2(DMD):c.-8T>A rs113726961
NM_004006.2(DMD):c.-96261C>T rs587780919
NM_004006.2(DMD):c.10087-20C>T rs41303187
NM_004006.2(DMD):c.10789C>T (p.Leu3597=) rs1800281
NM_004006.2(DMD):c.1225A>T (p.Thr409Ser) rs34155804
NM_004006.2(DMD):c.1483-7C>G rs112463388
NM_004006.2(DMD):c.1554T>A (p.Asp518Glu) rs61733587
NM_004006.2(DMD):c.1635A>G (p.Arg545=) rs5927083
NM_004006.2(DMD):c.1666G>A (p.Asp556Asn) rs182708940
NM_004006.2(DMD):c.1869C>T (p.Leu623=) rs1800267
NM_004006.2(DMD):c.1997C>T (p.Ser666Leu) rs34563188
NM_004006.2(DMD):c.2143A>T (p.Thr715Ser) rs16998350
NM_004006.2(DMD):c.2168+13T>C rs228373
NM_004006.2(DMD):c.2261G>T (p.Gly754Val) rs151242451
NM_004006.2(DMD):c.2293-15G>C rs369384547
NM_004006.2(DMD):c.2380+11G>A rs183120304
NM_004006.2(DMD):c.2391T>G (p.Asn797Lys) rs72468681
NM_004006.2(DMD):c.2457A>C (p.Leu819=) rs72468680
NM_004006.2(DMD):c.2490C>T (p.Asn830=) rs72468679
NM_004006.2(DMD):c.2569C>T (p.Pro857Ser) rs552275776
NM_004006.2(DMD):c.2623-11C>G rs1028360
NM_004006.2(DMD):c.2645G>A (p.Gly882Asp) rs228406
NM_004006.2(DMD):c.2745A>C (p.Thr915=) rs149922633
NM_004006.2(DMD):c.3021G>A (p.Ser1007=) rs1800268
NM_004006.2(DMD):c.31+36946C>T rs186833917
NM_004006.2(DMD):c.31+36949C>T rs182597890
NM_004006.2(DMD):c.3276+17A>T rs184220727
NM_004006.2(DMD):c.3406A>T (p.Thr1136Ser) rs3827462
NM_004006.2(DMD):c.3432+2036A>C rs182575709
NM_004006.2(DMD):c.3603+3delA rs5902031
NM_004006.2(DMD):c.3603+8A>G rs193249735
NM_004006.2(DMD):c.3705C>T (p.Ala1235=) rs143628111
NM_004006.2(DMD):c.3734C>T (p.Thr1245Ile) rs1800269
NM_004006.2(DMD):c.3787-18T>C rs72468656
NM_004006.2(DMD):c.38G>A (p.Arg13Lys) rs587780918
NM_004006.2(DMD):c.3970C>T (p.Arg1324Cys) rs143184877
NM_004006.2(DMD):c.4162T>G (p.Phe1388Val) rs28715870
NM_004006.2(DMD):c.4233+2C>T rs147474070
NM_004006.2(DMD):c.4234-13A>G rs41303181
NM_004006.2(DMD):c.4275A>G (p.Glu1425=) rs72468647
NM_004006.2(DMD):c.4344+17A>T rs72468646
NM_004006.2(DMD):c.4878G>T (p.Val1626=) rs61733574
NM_004006.2(DMD):c.5016T>A (p.Asn1672Lys) rs16990264
NM_004006.2(DMD):c.5182C>T (p.Arg1728Cys) rs34102501
NM_004006.2(DMD):c.5234G>A (p.Arg1745His) rs1801187
NM_004006.2(DMD):c.5586+18A>G rs189522063
NM_004006.2(DMD):c.5586+9G>A rs200025478
NM_004006.2(DMD):c.5724T>C (p.Asp1908=) rs143159113
NM_004006.2(DMD):c.6322C>T (p.Arg2108Cys) rs16990169
NM_004006.2(DMD):c.6463C>T (p.Arg2155Trp) rs1800273
NM_004006.2(DMD):c.6614+3294G>A rs5972467
NM_004006.2(DMD):c.6828C>T (p.Pro2276=) rs72466595
NM_004006.2(DMD):c.7096C>A (p.Gln2366Lys) rs1800275
NM_004006.2(DMD):c.7472A>G (p.Gln2491Arg) rs147694734
NM_004006.2(DMD):c.7476T>C (p.Val2492=) rs142153424
NM_004006.2(DMD):c.7542+13A>G rs72466585
NM_004006.2(DMD):c.7728T>C (p.Asn2576=) rs1801188
NM_004006.2(DMD):c.8027+11C>T rs2270672
NM_004006.2(DMD):c.802T>C (p.Leu268=) rs1800264
NM_004006.2(DMD):c.832-17C>A rs72470514
NM_004006.2(DMD):c.832-18C>G rs72470515
NM_004006.2(DMD):c.832-3C>T rs777492476
NM_004006.2(DMD):c.837G>A (p.Thr279=) rs1800265
NM_004006.2(DMD):c.8571T>C (p.Thr2857=) rs72466570
NM_004006.2(DMD):c.8668+19A>G rs148241865
NM_004006.2(DMD):c.8729A>T (p.Glu2910Val) rs41305353
NM_004006.2(DMD):c.8734A>G (p.Asn2912Asp) rs1800278
NM_004006.2(DMD):c.8762A>G (p.His2921Arg) rs1800279
NM_004006.2(DMD):c.8810A>G (p.Gln2937Arg) rs1800280
NM_004006.2(DMD):c.9085-15539G>A rs143848649
NM_004006.2(DMD):c.9225-301T>C rs73617063
NM_004006.2(DMD):c.9225-645T>C rs73617065
NM_004006.2(DMD):c.923C>T (p.Thr308Ile) rs145064612
NM_004006.2(DMD):c.93+5593T>A rs34352997
NM_004006.2(DMD):c.93+5601G>T rs34892244
NM_004006.2(DMD):c.94-9dupT rs3834997
NM_004006.2(DMD):c.9649+15T>C rs2293668
NM_004010.3(DMD):c.2012-3T>C rs147931243

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