Annotation Detail
Information
- Associated Genes
- HTR2A
- Associated Variants
-
HTR2A c.614-2211T>C
(
ENST00000543956.5,
ENST00000542664.4 )
HTR2A c.614-2211T>C ( ENST00000542664.4, ENST00000543956.5 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000621.5(HTR2A):c.614-2211T>C AND not specified
- ClinVar Allele ID
- 227777
- ClinVar RefSeq Alternation Syntax
- NM_000621.5:c.614-2211T>C
- ClinVar RefSeq Alternation Syntax
- NM_001378924.1:c.614-2211T>C
- ClinVar RefSeq Alternation Syntax
- NM_001165947.5:c.125-2211T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-03-09
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000600276
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs