ClinVar Miner

List of variants in gene DMD studied for Cardiovascular phenotype

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Total variants: 135
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HGVS dbSNP
LRG_199t1:c.2645A>G
LRG_199t1:c.7096A>C
LRG_199t1:c.8810G>A
NM_000109.3(DMD):c.7547G>A (p.Arg2516His) rs151244052
NM_000109.3(DMD):c.9658T>C (p.Phe3220Leu) rs141392048
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.10940G>A (p.Ser3647Asn) rs759642119
NM_004006.2(DMD):c.1095A>C (p.Gln365His) rs1800266
NM_004006.2(DMD):c.1132C>G (p.Gln378Glu) rs1556876203
NM_004006.2(DMD):c.1225A>T (p.Thr409Ser) rs34155804
NM_004006.2(DMD):c.1309G>C (p.Ala437Pro) rs748964279
NM_004006.2(DMD):c.1337A>G (p.His446Arg) rs72468699
NM_004006.2(DMD):c.1382A>G (p.Asn461Ser) rs775115784
NM_004006.2(DMD):c.1481A>G (p.Lys494Arg) rs1556853018
NM_004006.2(DMD):c.1513G>C (p.Val505Leu) rs140340626
NM_004006.2(DMD):c.1554T>A (p.Asp518Glu) rs61733587
NM_004006.2(DMD):c.1575A>G (p.Ala525=) rs144372300
NM_004006.2(DMD):c.1603-4C>G rs377223643
NM_004006.2(DMD):c.1635A>G (p.Arg545=) rs5927083
NM_004006.2(DMD):c.1704+3G>A rs773123973
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.1749C>G (p.Asn583Lys) rs775846754
NM_004006.2(DMD):c.1812C>T (p.Ala604=) rs140919039
NM_004006.2(DMD):c.1869C>T (p.Leu623=) rs1800267
NM_004006.2(DMD):c.1882_1884del (p.Leu628del) rs767034345
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.2084T>G (p.Leu695Arg) rs1556780761
NM_004006.2(DMD):c.2143A>T (p.Thr715Ser) rs16998350
NM_004006.2(DMD):c.2222T>C (p.Val741Ala) rs886039135
NM_004006.2(DMD):c.2260G>T (p.Gly754Cys) rs369017141
NM_004006.2(DMD):c.2323A>G (p.Arg775Gly) rs886038905
NM_004006.2(DMD):c.2331G>C (p.Leu777=) rs369659071
NM_004006.2(DMD):c.2331G>T (p.Leu777=) rs369659071
NM_004006.2(DMD):c.2391T>G (p.Asn797Lys) rs72468681
NM_004006.2(DMD):c.2490C>T (p.Asn830=) rs72468679
NM_004006.2(DMD):c.2539A>G (p.Thr847Ala) rs138145424
NM_004006.2(DMD):c.2569C>T (p.Pro857Ser) rs552275776
NM_004006.2(DMD):c.2575A>T (p.Thr859Ser) rs187926894
NM_004006.2(DMD):c.2617T>C (p.Cys873Arg) rs200872948
NM_004006.2(DMD):c.2745A>C (p.Thr915=) rs149922633
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.2973G>A (p.Glu991=) rs780454571
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.3232C>T (p.Leu1078Phe) rs375329908
NM_004006.2(DMD):c.3360G>A (p.Glu1120=) rs754467083
NM_004006.2(DMD):c.3406A>T (p.Thr1136Ser) rs3827462
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.3825G>A (p.Leu1275=) rs1379237787
NM_004006.2(DMD):c.3951G>A (p.Glu1317=) rs199643655
NM_004006.2(DMD):c.3970C>T (p.Arg1324Cys) rs143184877
NM_004006.2(DMD):c.3982C>G (p.Gln1328Glu) rs745640786
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.4233+2C>T rs147474070
NM_004006.2(DMD):c.4275A>G (p.Glu1425=) rs72468647
NM_004006.2(DMD):c.4283A>G (p.Lys1428Arg) rs371585389
NM_004006.2(DMD):c.4296G>T (p.Gln1432His) rs747262903
NM_004006.2(DMD):c.4345-4dup rs1557322418
NM_004006.2(DMD):c.4510C>T (p.His1504Tyr) rs1469008607
NM_004006.2(DMD):c.4529A>G (p.Lys1510Arg) rs72468638
NM_004006.2(DMD):c.4684A>G (p.Arg1562Gly) rs771425504
NM_004006.2(DMD):c.468A>C (p.Val156=) rs886044031
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.5048C>G (p.Thr1683Ser) rs146420425
NM_004006.2(DMD):c.5163G>C (p.Lys1721Asn) rs72468630
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.5216C>A (p.Ala1739Glu) rs200740165
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.5270T>C (p.Ile1757Thr) rs201516290
NM_004006.2(DMD):c.5349G>A (p.Leu1783=) rs886039049
NM_004006.2(DMD):c.5390T>C (p.Leu1797Pro) rs750303298
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.562T>G (p.Cys188Gly) rs1557047949
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.5758C>T (p.Gln1920Ter) rs1057520764
NM_004006.2(DMD):c.5864G>A (p.Arg1955His) rs200455300
NM_004006.2(DMD):c.5984A>T (p.Tyr1995Phe) rs147927593
NM_004006.2(DMD):c.6067C>T (p.Leu2023Phe) rs869312948
NM_004006.2(DMD):c.6143G>A (p.Ser2048Asn) rs200494003
NM_004006.2(DMD):c.6200C>T (p.Thr2067Met) rs1405599353
NM_004006.2(DMD):c.6319C>T (p.Arg2107Trp) rs770711808
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.6471T>A (p.Thr2157=) rs377080659
NM_004006.2(DMD):c.6571C>T (p.Arg2191Trp) rs149322279
NM_004006.2(DMD):c.694A>C (p.Ile232Leu) rs758447768
NM_004006.2(DMD):c.7150T>C (p.Ser2384Pro) rs1351313240
NM_004006.2(DMD):c.7151C>A (p.Ser2384Tyr) rs185706283
NM_004006.2(DMD):c.7183G>A (p.Ala2395Thr) rs72466590
NM_004006.2(DMD):c.7237G>A (p.Val2413Ile) rs373604575
NM_004006.2(DMD):c.7243C>T (p.Arg2415Cys) rs139395045
NM_004006.2(DMD):c.7281A>G (p.Leu2427=) rs886038872
NM_004006.2(DMD):c.7359A>G (p.Glu2453=) rs780283825
NM_004006.2(DMD):c.7429C>T (p.Arg2477Trp) rs759274835
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.74T>C (p.Val25Ala) rs886039061
NM_004006.2(DMD):c.7521C>T (p.Asn2507=) rs112516305
NM_004006.2(DMD):c.7712G>T (p.Arg2571Leu) rs371588290
NM_004006.2(DMD):c.7728T>C (p.Asn2576=) rs1801188
NM_004006.2(DMD):c.7820A>T (p.Lys2607Met) rs72466581
NM_004006.2(DMD):c.802T>C (p.Leu268=) rs1800264
NM_004006.2(DMD):c.8053G>A (p.Glu2685Lys) rs748937055
NM_004006.2(DMD):c.8076A>G (p.Gln2692=) rs144518527
NM_004006.2(DMD):c.8212T>C (p.Trp2738Arg) rs372600090
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.837G>A (p.Thr279=) rs1800265
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.8767G>T (p.Ala2923Ser) rs116283249
NM_004006.2(DMD):c.8824G>C (p.Ala2942Pro) rs755127162
NM_004006.2(DMD):c.8974G>A (p.Val2992Met) rs201691420
NM_004006.2(DMD):c.8976G>A (p.Val2992=) rs916865376
NM_004006.2(DMD):c.9165G>A (p.Thr3055=) rs137905486
NM_004006.2(DMD):c.9291C>T (p.Asp3097=) rs796934165
NM_004006.2(DMD):c.9486G>A (p.Glu3162=) rs370724251
NM_004006.2(DMD):c.9804A>G (p.Gln3268=) rs12690372
NM_004006.2(DMD):c.9931G>A (p.Ala3311Thr) rs1348920866

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