Annotation Detail
Information
- Associated Genes
- SLC2A1
- Associated Variants
-
SLC2A1 p.Arg89His (p.R89H)
(
ENST00000426263.10,
ENST00000674765.1 )
SLC2A1 p.Arg89His (p.R89H) ( ENST00000426263.10, ENST00000674765.1 ) - Associated Disease
- Epilepsy, idiopathic generalized, susceptibility to, 12
- Source Database
- ClinVar
- Description
- NM_006516.4(SLC2A1):c.266G>A (p.Arg89His) AND Epilepsy, idiopathic generalized, susceptibility to, 12
- ClinVar Allele ID
- 1349794
- ClinVar RefSeq Alternation Syntax
- NM_006516.4:c.266G>A
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2023-04-11
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003446960
- ClinVar Disease
- Epilepsy, idiopathic generalized, susceptibility to, 12
- Observed Origin Sample
- germline
Drugs