ClinVar Miner

List of variants reported as uncertain significance for childhood-onset nemaline myopathy by Genome Diagnostics Laboratory,University Medical Center Utrecht

Included ClinVar conditions (12):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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NM_001101362.2(KBTBD13):c.251G>C (p.Cys84Ser) rs999785767

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