Annotation Detail
Information
- Associated Genes
- ADRB2
- Associated Variants
-
ADRB2 p.Gly351= (p.G351=)
(
ENST00000305988.6 )
ADRB2 p.Gly351= (p.G351=) ( ENST00000305988.6 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000024.6(ADRB2):c.1053G>C (p.Gly351=) AND not provided
- ClinVar Allele ID
- 1227197
- ClinVar RefSeq Alternation Syntax
- NM_000024.6:c.1053G>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-11-10
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001639295
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs