ClinVar Miner

List of variants in gene DMD reported as pathogenic for Motor delay; Muscle weakness; Muscle cramps; EMG abnormality; EMG: myopathic abnormalities; Calf muscle hypertrophy

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP
NM_004006.2(DMD):c.1637G>A (p.Trp546Ter) rs1057518962

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