ClinVar Miner

List of variants reported as benign for Duchenne muscular dystrophy

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 140
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HGVS dbSNP
NM_004006.2(DMD):c.10128A>G (p.Leu3376=) rs755438733
NM_004006.2(DMD):c.10262+1G>A rs145603325
NM_004006.2(DMD):c.1028G>A (p.Arg343His) rs61733589
NM_004006.2(DMD):c.10789C>T (p.Leu3597=) rs1800281
NM_004006.2(DMD):c.10836C>T (p.Ser3612=) rs148590546
NM_004006.2(DMD):c.1095A>C (p.Gln365His) rs1800266
NM_004006.2(DMD):c.1184G>A (p.Arg395Gln) rs148511512
NM_004006.2(DMD):c.1225A>T (p.Thr409Ser) rs34155804
NM_004006.2(DMD):c.1252A>T (p.Thr418Ser) rs201341211
NM_004006.2(DMD):c.1318G>A (p.Glu440Lys) rs189143447
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.1718C>T (p.Ala573Val) rs5972599
NM_004006.2(DMD):c.1731A>T (p.Glu577Asp) rs150199251
NM_004006.2(DMD):c.1809G>A (p.Leu603=) rs192176661
NM_004006.2(DMD):c.1813-3C>A rs181399181
NM_004006.2(DMD):c.1824G>A (p.Ala608=) rs151013182
NM_004006.2(DMD):c.1848C>A (p.Ser616=) rs376024929
NM_004006.2(DMD):c.1869C>G (p.Leu623=) rs1800267
NM_004006.2(DMD):c.1869C>T (p.Leu623=) rs1800267
NM_004006.2(DMD):c.1888A>G (p.Thr630Ala) rs72468692
NM_004006.2(DMD):c.1997C>T (p.Ser666Leu) rs34563188
NM_004006.2(DMD):c.2096C>G (p.Ala699Gly) rs202008454
NM_004006.2(DMD):c.2143A>T (p.Thr715Ser) rs16998350
NM_004006.2(DMD):c.2199C>T (p.Ser733=) rs149882431
NM_004006.2(DMD):c.2261G>T (p.Gly754Val) rs151242451
NM_004006.2(DMD):c.2273A>C (p.Asp758Ala) rs750526692
NM_004006.2(DMD):c.2331G>C (p.Leu777=) rs369659071
NM_004006.2(DMD):c.2380+10C>T rs372330460
NM_004006.2(DMD):c.2381-3T>C rs147931243
NM_004006.2(DMD):c.2386G>A (p.Val796Ile) rs139726281
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.2623-9A>G rs200997841
NM_004006.2(DMD):c.2645G>A (p.Gly882Asp) rs228406
NM_004006.2(DMD):c.2667A>T (p.Arg889=) rs759593799
NM_004006.2(DMD):c.2745A>C (p.Thr915=) rs149922633
NM_004006.2(DMD):c.2824A>G (p.Met942Val) rs371648742
NM_004006.2(DMD):c.2827C>T (p.Arg943Cys) rs199986217
NM_004006.2(DMD):c.2884C>G (p.Leu962Val) rs150959827
NM_004006.2(DMD):c.2971G>C (p.Glu991Gln) rs72468667
NM_004006.2(DMD):c.3020C>T (p.Ser1007Leu) rs144732570
NM_004006.2(DMD):c.3021G>A (p.Ser1007=) rs1800268
NM_004006.2(DMD):c.3217G>A (p.Glu1073Lys) rs398123931
NM_004006.2(DMD):c.3326A>T (p.Asn1109Ile) rs200596739
NM_004006.2(DMD):c.333T>C (p.Ile111=) rs138909301
NM_004006.2(DMD):c.3406A>T (p.Thr1136Ser) rs3827462
NM_004006.2(DMD):c.3419A>G (p.His1140Arg) rs201297190
NM_004006.2(DMD):c.3472A>G (p.Lys1158Glu) rs182728059
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.3794G>C (p.Trp1265Ser) rs200213555
NM_004006.2(DMD):c.3941G>A (p.Arg1314Gln) rs752767880
NM_004006.2(DMD):c.3951G>A (p.Glu1317=) rs199643655
NM_004006.2(DMD):c.3960A>G (p.Pro1320=) rs765256995
NM_004006.2(DMD):c.3970C>T (p.Arg1324Cys) rs143184877
NM_004006.2(DMD):c.4125T>C (p.Thr1375=) rs144329742
NM_004006.2(DMD):c.4162T>G (p.Phe1388Val) rs28715870
NM_004006.2(DMD):c.4206C>T (p.Asp1402=) rs766668051
NM_004006.2(DMD):c.4233+2C>T rs147474070
NM_004006.2(DMD):c.4275A>G (p.Glu1425=) rs72468647
NM_004006.2(DMD):c.4529A>G (p.Lys1510Arg) rs72468638
NM_004006.2(DMD):c.4721G>A (p.Arg1574His) rs755206033
NM_004006.2(DMD):c.4845+10A>G rs199958675
NM_004006.2(DMD):c.4876G>A (p.Val1626Met) rs776998846
NM_004006.2(DMD):c.4878G>T (p.Val1626=) rs61733574
NM_004006.2(DMD):c.5010G>T (p.Trp1670Cys) rs727503828
NM_004006.2(DMD):c.5016T>A (p.Asn1672Lys) rs16990264
NM_004006.2(DMD):c.5026-7A>G rs398123976
NM_004006.2(DMD):c.5163G>C (p.Lys1721Asn) rs72468630
NM_004006.2(DMD):c.5181A>T (p.Ile1727=) rs200887855
NM_004006.2(DMD):c.5182C>T (p.Arg1728Cys) rs34102501
NM_004006.2(DMD):c.5203C>T (p.Arg1735Cys) rs147904018
NM_004006.2(DMD):c.5234G>A (p.Arg1745His) rs1801187
NM_004006.2(DMD):c.5265C>T (p.Pro1755=) rs145515413
NM_004006.2(DMD):c.5485C>G (p.Gln1829Glu) rs754765424
NM_004006.2(DMD):c.5620G>A (p.Glu1874Lys) rs142441725
NM_004006.2(DMD):c.5701G>A (p.Ala1901Thr) rs201302282
NM_004006.2(DMD):c.5724T>C (p.Asp1908=) rs143159113
NM_004006.2(DMD):c.5984A>T (p.Tyr1995Phe) rs147927593
NM_004006.2(DMD):c.606C>T (p.Ile202=) rs138335295
NM_004006.2(DMD):c.6132T>C (p.Ser2044=) rs761338933
NM_004006.2(DMD):c.6140A>G (p.Gln2047Arg) rs773782786
NM_004006.2(DMD):c.6143G>A (p.Ser2048Asn) rs200494003
NM_004006.2(DMD):c.6291-10T>C rs758023750
NM_004006.2(DMD):c.6322C>T (p.Arg2108Cys) rs16990169
NM_004006.2(DMD):c.6414T>C (p.His2138=) rs753999355
NM_004006.2(DMD):c.6463C>T (p.Arg2155Trp) rs1800273
NM_004006.2(DMD):c.6471T>A (p.Thr2157=) rs377080659
NM_004006.2(DMD):c.6483A>G (p.Thr2161=) rs776054222
NM_004006.2(DMD):c.6571C>T (p.Arg2191Trp) rs149322279
NM_004006.2(DMD):c.6614+7C>T rs180719577
NM_004006.2(DMD):c.6614+8G>A rs377508818
NM_004006.2(DMD):c.6732G>C (p.Gln2244His) rs142531761
NM_004006.2(DMD):c.6828C>T (p.Pro2276=) rs72466595
NM_004006.2(DMD):c.696C>G (p.Ile232Met) rs145668843
NM_004006.2(DMD):c.7085C>A (p.Pro2362Gln) rs141151675
NM_004006.2(DMD):c.7096C>A (p.Gln2366Lys) rs1800275
NM_004006.2(DMD):c.7130C>T (p.Pro2377Leu) rs201262489
NM_004006.2(DMD):c.7151C>A (p.Ser2384Tyr) rs185706283
NM_004006.2(DMD):c.7243C>T (p.Arg2415Cys) rs139395045
NM_004006.2(DMD):c.7244G>A (p.Arg2415His) rs373749120
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.7521C>T (p.Asn2507=) rs112516305
NM_004006.2(DMD):c.7555G>A (p.Asp2519Asn) rs771877780
NM_004006.2(DMD):c.7596C>T (p.Thr2532=) rs778412539
NM_004006.2(DMD):c.7653G>A (p.Thr2551=) rs368803197
NM_004006.2(DMD):c.7728T>C (p.Asn2576=) rs1801188
NM_004006.2(DMD):c.8027+7A>T rs72466580
NM_004006.2(DMD):c.802T>C (p.Leu268=) rs1800264
NM_004006.2(DMD):c.8138A>G (p.Asn2713Ser) rs758633794
NM_004006.2(DMD):c.821A>G (p.Tyr274Cys) rs745868830
NM_004006.2(DMD):c.8226A>G (p.Gln2742=) rs746514008
NM_004006.2(DMD):c.8255A>G (p.Tyr2752Cys) rs373832446
NM_004006.2(DMD):c.8308G>A (p.Asp2770Asn) rs138399787
NM_004006.2(DMD):c.837G>A (p.Thr279=) rs1800265
NM_004006.2(DMD):c.8436T>C (p.Leu2812=) rs139365076
NM_004006.2(DMD):c.8571T>C (p.Thr2857=) rs72466570
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.8852G>A (p.Arg2951His) rs72466567
NM_004006.2(DMD):c.8973C>T (p.Asn2991=) rs772306909
NM_004006.2(DMD):c.9165G>A (p.Thr3055=) rs137905486
NM_004006.2(DMD):c.923C>T (p.Thr308Ile) rs145064612
NM_004006.2(DMD):c.94-16dup rs3834997
NM_004006.2(DMD):c.94-3C>T rs373907950
NM_004006.2(DMD):c.94-9T>A rs3764764
NM_004006.2(DMD):c.9479G>A (p.Arg3160His) rs771392678
NM_004006.2(DMD):c.9486G>A (p.Glu3162=) rs370724251
NM_004006.2(DMD):c.9682T>C (p.Phe3228Leu) rs141392048
NM_004006.2(DMD):c.9804A>G (p.Gln3268=) rs12690372
NM_004006.2(DMD):c.9888C>T (p.Pro3296=) rs146543659

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