Annotation Detail
Information
- Associated Genes
- HTR2A
- Associated Variants
-
HTR2A c.-329+609G>A
HTR2A c.-329+609G>A - Associated Disease
- Obsessive-compulsive disorder, susceptibility to
- Source Database
- ClinVar
- Description
- NM_001378924.1(HTR2A):c.-329+609G>A AND Obsessive-compulsive disorder, susceptibility to
- ClinVar Allele ID
- 504813
- ClinVar RefSeq Alternation Syntax
- NM_001378924.1:c.-329+609G>A
- Clinical Significance Description
- risk factor
- Clinical Significance Last Update
- 2004-09-15
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001836848
- ClinVar Disease
- Obsessive-compulsive disorder, susceptibility to
- Observed Origin Sample
- germline
- Pubmed
- 12476319
- Pubmed
- 15364038
- Pubmed
- 9635956
Drugs