Annotation Detail
Information
- Associated Genes
- ADRB1
- Associated Variants
-
ADRB1 p.Ser49Gly (p.S49G)
(
ENST00000369295.4 )
ADRB1 p.Ser49Gly (p.S49G) ( ENST00000369295.4 ) - Associated Disease
- ADRB1-related disorder
- Source Database
- ClinVar
- Description
- NM_000684.3(ADRB1):c.145A>G (p.Ser49Gly) AND ADRB1-related disorder
- ClinVar Allele ID
- 32786
- ClinVar RefSeq Alternation Syntax
- NM_000684.3:c.145A>G
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2019-10-28
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV003974845
- ClinVar Disease
- ADRB1-related disorder
- Observed Origin Sample
- germline
Drugs