ClinVar Miner

List of variants reported as benign for Duchenne muscular dystrophy

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Total variants: 21
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HGVS dbSNP
NM_000109.4(DMD):c.1294G>A (p.Glu432Lys) rs189143447
NM_000109.4(DMD):c.70-16dup rs3834997
NM_000109.4(DMD):c.7547G>A (p.Arg2516His) rs151244052
NM_000109.4(DMD):c.8786G>A (p.Arg2929Gln) rs1800280
NM_000109.4(DMD):c.9658T>C (p.Phe3220Leu) rs141392048
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.3021G>A (p.Ser1007=) rs1800268
NM_004006.2(DMD):c.3406A>T (p.Thr1136Ser) rs3827462
NM_004006.2(DMD):c.3734C>T (p.Thr1245Ile) rs1800269
NM_004006.2(DMD):c.4206C>T (p.Asp1402=) rs766668051
NM_004006.2(DMD):c.5026-7A>G rs398123976
NM_004006.2(DMD):c.5234G>A (p.Arg1745His) rs1801187
NM_004006.2(DMD):c.6463C>T (p.Arg2155Trp) rs1800273
NM_004006.2(DMD):c.6483A>G (p.Thr2161=) rs776054222
NM_004006.2(DMD):c.7183G>A (p.Ala2395Thr) rs72466590
NM_004006.2(DMD):c.7728T>C (p.Asn2576=) rs1801188
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_004013.2(DMD):c.-285= rs1800275

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