Annotation Detail
Information
- Associated Genes
- CLCN1
- Associated Variants
-
CLCN1 p.Gln552Arg (p.Q552R)
(
ENST00000343257.7,
ENST00000650516.2 )
CLCN1 p.Gln552Arg (p.Q552R) ( ENST00000343257.7, ENST00000650516.2 ) - Associated Disease
- Congenital myotonia, autosomal dominant form
- Source Database
- ClinVar
- Description
- NM_000083.3(CLCN1):c.1655A>G (p.Gln552Arg) AND Congenital myotonia, autosomal dominant form
- ClinVar Allele ID
- 32577
- ClinVar RefSeq Alternation Syntax
- NR_046453.2:n.1610A>G
- ClinVar RefSeq Alternation Syntax
- NM_000083.3:c.1655A>G
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2017-06-23
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001253100
- ClinVar Disease
- Congenital myotonia, autosomal dominant form
- Observed Origin Sample
- germline
Drugs