ClinVar Miner

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

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Gene type:
ClinVar version:
Total variants: 20
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NM_004006.2(DMD):c.1047A>T (p.Glu349Asp) rs1044325754
NM_004006.2(DMD):c.1310C>G (p.Ala437Gly) rs1556875180
NM_004006.2(DMD):c.1331+2dup rs1556875106
NM_004006.2(DMD):c.139G>T (p.Gly47Trp) rs1557084183
NM_004006.2(DMD):c.2176G>T (p.Val726Phe) rs886044365
NM_004006.2(DMD):c.3239A>G (p.Asp1080Gly) rs886043493
NM_004006.2(DMD):c.419T>G (p.Leu140Arg) rs1557052675
NM_004006.2(DMD):c.4409G>A (p.Arg1470His) rs752129019
NM_004006.2(DMD):c.5518G>C (p.Asp1840His) rs905571950
NM_004006.2(DMD):c.6196G>T (p.Ala2066Ser) rs1468473458
NM_004006.2(DMD):c.6290+5G>A rs886043467
NM_004006.2(DMD):c.6762G>C (p.Lys2254Asn) rs1569516110
NM_004006.2(DMD):c.711A>C (p.Gln237His) rs778632674
NM_004006.2(DMD):c.7201-4A>G rs1556917126
NM_004006.2(DMD):c.7919C>G (p.Ala2640Gly) rs146020545
NM_004006.2(DMD):c.8138A>G (p.Asn2713Ser) rs758633794
NM_004006.2(DMD):c.8828C>T (p.Thr2943Met) rs751810893
NM_004006.2(DMD):c.9352G>T (p.Ala3118Ser) rs200928985
NM_004006.3(DMD):c.3603+2_3603+3insTA rs1603633860
NM_004006.3(DMD):c.8015G>A (p.Ser2672Asn) rs771081514

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