ClinVar Miner

List of variants studied for childhood-onset nemaline myopathy by Institute of Human Genetics,Klinikum rechts der Isar

Included ClinVar conditions (12):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 2
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NM_001100.3(ACTA1):c.442G>A (p.Gly148Ser) rs398123563
NM_001271208.2(NEB):c.9619-2A>G rs375145370

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