ClinVar Miner

List of variants in gene DMD reported as uncertain significance for Cardiovascular phenotype

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Total variants: 53
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HGVS dbSNP
NM_004006.2(DMD):c.10262+1G>A rs145603325
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.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.1603-4C>G rs377223643
NM_004006.2(DMD):c.1704+3G>A rs773123973
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.1879_1881CTT[1] (p.Leu628del) rs767034345
NM_004006.2(DMD):c.2084T>G (p.Leu695Arg) rs1556780761
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.2539A>G (p.Thr847Ala) rs138145424
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.2884C>G (p.Leu962Val) rs150959827
NM_004006.2(DMD):c.3232C>T (p.Leu1078Phe) rs375329908
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.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.4684A>G (p.Arg1562Gly) rs771425504
NM_004006.2(DMD):c.5048C>G (p.Thr1683Ser) rs146420425
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.5270T>C (p.Ile1757Thr) rs201516290
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.562T>G (p.Cys188Gly) rs1557047949
NM_004006.2(DMD):c.5701G>A (p.Ala1901Thr) rs201302282
NM_004006.2(DMD):c.5864G>A (p.Arg1955His) rs200455300
NM_004006.2(DMD):c.6067C>T (p.Leu2023Phe) rs869312948
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.694A>C (p.Ile232Leu) rs758447768
NM_004006.2(DMD):c.7150T>C (p.Ser2384Pro) rs1351313240
NM_004006.2(DMD):c.7237G>A (p.Val2413Ile) rs373604575
NM_004006.2(DMD):c.7429C>T (p.Arg2477Trp) rs759274835
NM_004006.2(DMD):c.74T>C (p.Val25Ala) rs886039061
NM_004006.2(DMD):c.7712G>T (p.Arg2571Leu) rs371588290
NM_004006.2(DMD):c.7820A>T (p.Lys2607Met) rs72466581
NM_004006.2(DMD):c.8053G>A (p.Glu2685Lys) rs748937055
NM_004006.2(DMD):c.8212T>C (p.Trp2738Arg) rs372600090
NM_004006.2(DMD):c.8255A>G (p.Tyr2752Cys) rs373832446
NM_004006.2(DMD):c.8824G>C (p.Ala2942Pro) rs755127162
NM_004006.2(DMD):c.9931G>A (p.Ala3311Thr) rs1348920866

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