ClinVar Miner

List of variants in gene DMD reported as likely benign for Dilated cardiomyopathy 3B

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Gene type:
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Total variants: 36
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HGVS dbSNP
NM_004006.2(DMD):c.*1285C>A rs142110702
NM_004006.2(DMD):c.*1447A>G rs3361
NM_004006.2(DMD):c.*1562_*1565dupTAAG rs758612124
NM_004006.2(DMD):c.*1638A>G rs142520583
NM_004006.2(DMD):c.*1783A>G rs7886658
NM_004006.2(DMD):c.*2037_*2038dup rs200703281
NM_004006.2(DMD):c.*2039C>A rs72466523
NM_004006.2(DMD):c.-114dup rs72470542
NM_004006.2(DMD):c.-8T>A rs113726961
NM_004006.2(DMD):c.1225A>T (p.Thr409Ser) rs34155804
NM_004006.2(DMD):c.1635A>G (p.Arg545=) rs5927083
NM_004006.2(DMD):c.1869C>T (p.Leu623=) rs1800267
NM_004006.2(DMD):c.2168+13T>C rs228373
NM_004006.2(DMD):c.2623-11C>G rs1028360
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.4162T>G (p.Phe1388Val) rs28715870
NM_004006.2(DMD):c.4234-13A>G rs41303181
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.4878G>T (p.Val1626=) rs61733574
NM_004006.2(DMD):c.5016T>A (p.Asn1672Lys) rs16990264
NM_004006.2(DMD):c.5234G>A (p.Arg1745His) rs1801187
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.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.837G>A (p.Thr279=) rs1800265
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.94-16dup rs3834997
NM_004006.2(DMD):c.9649+15T>C rs2293668

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