Annotation Detail
Information
- Associated Genes
- HTR1A
- Associated Variants
-
HTR1A p.Arg220Leu (p.R220L)
(
ENST00000323865.5 )
HTR1A p.Arg220Leu (p.R220L) ( ENST00000323865.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000524.4(HTR1A):c.659G>T (p.Arg220Leu) AND not provided
- ClinVar Allele ID
- 1306014
- ClinVar RefSeq Alternation Syntax
- NM_000524.4:c.659G>T
- Clinical Significance Description
- Benign/Likely benign
- Clinical Significance Last Update
- 2024-04-01
- Clinical Significance Review Status
- criteria provided, multiple submitters, no conflicts
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001755417
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs