ClinVar Miner

List of variants in gene DMD reported as benign by PreventionGenetics

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Gene type:
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Total variants: 26
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HGVS dbSNP
NM_004006.2(DMD):c.-8T>A rs113726961
NM_004006.2(DMD):c.1225A>T (p.Thr409Ser) rs34155804
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.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.3021G>A (p.Ser1007=) rs1800268
NM_004006.2(DMD):c.3567T>A (p.Thr1189=) rs370685748
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.4344+17A>T rs72468646
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.7476T>C (p.Val2492=) rs142153424
NM_004006.2(DMD):c.7542+13A>G rs72466585
NM_004006.2(DMD):c.7728T>C (p.Asn2576=) rs1801188
NM_004006.2(DMD):c.8027+11C>T rs2270672
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.94-9dupT rs3834997
NM_004006.2(DMD):c.9649+15T>C rs2293668

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