ClinVar Miner

List of variants reported as likely benign for Duchenne muscular dystrophy by Invitae

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Total variants: 43
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HGVS dbSNP
NM_000109.4(DMD):c.5425-11dup rs1557292841
NM_004006.2(DMD):c.10087-8C>A rs1261494456
NM_004006.2(DMD):c.1008G>A (p.Glu336=) rs1280118173
NM_004006.2(DMD):c.10122G>A (p.Lys3374=) rs1556037420
NM_004006.2(DMD):c.10308C>T (p.Arg3436=) rs780389106
NM_004006.2(DMD):c.10362T>C (p.Tyr3454=) rs1556028072
NM_004006.2(DMD):c.10620G>A (p.Pro3540=) rs72466538
NM_004006.2(DMD):c.1084T>C (p.Leu362=) rs1556876311
NM_004006.2(DMD):c.1473A>G (p.Gln491=) rs144303432
NM_004006.2(DMD):c.1542G>C (p.Val514=) rs1556834846
NM_004006.2(DMD):c.1704+8_1704+9del rs1556810175
NM_004006.2(DMD):c.1705-4G>A rs889499438
NM_004006.2(DMD):c.1920G>A (p.Thr640=) rs766895256
NM_004006.2(DMD):c.2400C>T (p.Ser800=) rs142115986
NM_004006.2(DMD):c.2508T>C (p.Tyr836=) rs886044674
NM_004006.2(DMD):c.2682C>T (p.Ser894=) rs398123904
NM_004006.2(DMD):c.2745A>G (p.Thr915=) rs149922633
NM_004006.2(DMD):c.2858C>T (p.Thr953Ile) rs142133195
NM_004006.2(DMD):c.2910C>T (p.Thr970=) rs765442122
NM_004006.2(DMD):c.3177C>T (p.Thr1059=) rs755632126
NM_004006.2(DMD):c.3924A>T (p.Ser1308=) rs1557357591
NM_004006.2(DMD):c.3988C>T (p.Leu1330=) rs1557357523
NM_004006.2(DMD):c.4314A>G (p.Gln1438=) rs985982212
NM_004006.2(DMD):c.4497G>A (p.Gln1499=) rs1417062461
NM_004006.2(DMD):c.4845+7C>T rs764100658
NM_004006.2(DMD):c.4881C>T (p.His1627=) rs886043184
NM_004006.2(DMD):c.5418T>C (p.Asn1806=) rs149543306
NM_004006.2(DMD):c.5448+7T>C rs1557294172
NM_004006.2(DMD):c.5577T>C (p.Asn1859=) rs372707022
NM_004006.2(DMD):c.5583C>T (p.Leu1861=) rs775837149
NM_004006.2(DMD):c.5688T>C (p.Ile1896=) rs1557291068
NM_004006.2(DMD):c.5739+8T>C rs1321625981
NM_004006.2(DMD):c.624C>A (p.Gly208=) rs768761464
NM_004006.2(DMD):c.651T>C (p.Asp217=) rs1556930849
NM_004006.2(DMD):c.6942A>G (p.Gly2314=) rs1556962536
NM_004006.2(DMD):c.7051T>C (p.Leu2351=) rs367747168
NM_004006.2(DMD):c.8355G>A (p.Lys2785=) rs772646759
NM_004006.2(DMD):c.861G>A (p.Glu287=) rs1284806719
NM_004006.2(DMD):c.8718G>A (p.Lys2906=) rs377178242
NM_004006.2(DMD):c.8847G>A (p.Lys2949=) rs185664502
NM_004006.2(DMD):c.888C>T (p.Phe296=) rs977310228
NM_004006.2(DMD):c.9651C>T (p.Tyr3217=) rs1313897024
NM_004006.2(DMD):c.999A>G (p.Ser333=) rs748489730

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