Annotation Detail
Information
- Associated Genes
- SLC2A1
- Associated Variants
-
SLC2A1 p.Arg92Trp (p.R92W)
(
ENST00000426263.10,
ENST00000674765.1 )
SLC2A1 p.Arg92Trp (p.R92W) ( ENST00000426263.10, ENST00000674765.1 ) - Associated Disease
- intellectual disability
- Source Database
- ClinVar
- Description
- NM_006516.4(SLC2A1):c.274C>T (p.Arg92Trp) AND Intellectual disability
- ClinVar Allele ID
- 31158
- ClinVar RefSeq Alternation Syntax
- NM_006516.4:c.274C>T
- Clinical Significance Description
- Likely pathogenic
- Clinical Significance Last Update
- 2019-02-13
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000850197
- ClinVar Disease
- Intellectual disability
- Observed Origin Sample
- unknown
Drugs