ClinVar Miner

List of variants in gene DMD reported as benign by Athena Diagnostics Inc

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 30
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HGVS dbSNP
NM_004006.2(DMD):c.1028G>A (p.Arg343His) rs61733589
NM_004006.2(DMD):c.1503A>G (p.Glu501=) rs770464589
NM_004006.2(DMD):c.1635A>G (p.Arg545=) rs5927083
NM_004006.2(DMD):c.1666G>A (p.Asp556Asn) rs182708940
NM_004006.2(DMD):c.1809G>A (p.Leu603=) rs192176661
NM_004006.2(DMD):c.1869C>T (p.Leu623=) rs1800267
NM_004006.2(DMD):c.1997C>T (p.Ser666Leu) rs34563188
NM_004006.2(DMD):c.2096C>G (p.Ala699Gly) rs202008454
NM_004006.2(DMD):c.2645G>A (p.Gly882Asp) rs228406
NM_004006.2(DMD):c.2971G>C (p.Glu991Gln) rs72468667
NM_004006.2(DMD):c.3705C>T (p.Ala1235=) rs143628111
NM_004006.2(DMD):c.3970C>T (p.Arg1324Cys) rs143184877
NM_004006.2(DMD):c.4072-3T>C rs751657094
NM_004006.2(DMD):c.4233+2C>T rs147474070
NM_004006.2(DMD):c.4878G>T (p.Val1626=) rs61733574
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.5984A>T (p.Tyr1995Phe) rs147927593
NM_004006.2(DMD):c.6463C>T (p.Arg2155Trp) rs1800273
NM_004006.2(DMD):c.6571C>T (p.Arg2191Trp) rs149322279
NM_004006.2(DMD):c.7096C>A (p.Gln2366Lys) rs1800275
NM_004006.2(DMD):c.7183G>A (p.Ala2395Thr) rs72466590
NM_004006.2(DMD):c.7397T>C (p.Met2466Thr) rs764330616
NM_004006.2(DMD):c.7728T>C (p.Asn2576=) rs1801188
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.8810A>G (p.Gln2937Arg) rs1800280
NM_004006.2(DMD):c.94-9dupT rs3834997

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