ClinVar Miner

List of variants reported as uncertain significance for Duchenne muscular dystrophy by Fulgent Genetics

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 10
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HGVS dbSNP
NM_004006.2(DMD):c.1687C>T (p.Arg563Cys) rs145739725
NM_004006.2(DMD):c.2330T>C (p.Leu777Pro) rs794727226
NM_004006.2(DMD):c.2912A>T (p.Asp971Val)
NM_004006.2(DMD):c.295A>G (p.Ile99Val) rs149428656
NM_004006.2(DMD):c.3344T>C (p.Ile1115Thr) rs748123444
NM_004006.2(DMD):c.5869C>T (p.Arg1957Trp) rs755477994
NM_004006.2(DMD):c.6409G>C (p.Glu2137Gln) rs1023328955
NM_004006.2(DMD):c.6839G>A (p.Ser2280Asn) rs1060502614
NM_004006.2(DMD):c.9352G>T (p.Ala3118Ser) rs200928985
NM_004006.2(DMD):c.9580A>C (p.Ile3194Leu) rs181517869

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