Annotation Detail
Information
- Associated Genes
- RAPSN
- Associated Variants
-
RAPSN c.-210A>G
RAPSN c.-210A>G - Associated Disease
- congenital myasthenic syndrome
- Source Database
- ClinVar
- Description
- NM_005055.5(RAPSN):c.-210A>G AND Congenital myasthenic syndrome
- ClinVar Allele ID
- 23090
- Clinical Significance Description
- Pathogenic
- Clinical Significance Last Update
- 2020-09-16
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000235034
- ClinVar Disease
- Congenital myasthenic syndrome
- Observed Origin Sample
- germline
Drugs