Annotation Detail
Information
- Associated Genes
- SLC6A4
- Associated Variants
-
SLC6A4 c.*463T>G
(
ENST00000650711.1,
ENST00000261707.7,
ENST00000401766.6 )
SLC6A4 c.*463T>G ( ENST00000261707.7, ENST00000401766.6, ENST00000650711.1 ) - Associated Disease
- Behavior disorder
- Source Database
- ClinVar
- Description
- NM_001045.6(SLC6A4):c.*463T>G AND Behavior disorder
- ClinVar Allele ID
- 343987
- ClinVar RefSeq Alternation Syntax
- NM_001045.6:c.*463T>G
- Clinical Significance Description
- Likely benign
- Clinical Significance Last Update
- 2016-06-14
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000308551
- ClinVar Disease
- Behavior disorder
- Observed Origin Sample
- germline
Drugs