Annotation Detail
Information
- Associated Genes
- HTR2A
- Associated Variants
-
HTR2A c.-329+609G>A
HTR2A c.-329+609G>A - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_001378924.1(HTR2A):c.-329+609G>A AND not specified
- ClinVar Allele ID
- 504813
- ClinVar RefSeq Alternation Syntax
- NM_001378924.1:c.-329+609G>A
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2018-03-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000605277
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs