Annotation Detail
Information
- Associated Genes
- DBH
- Associated Variants
-
DBH c.1024+192T>C
(
ENST00000393056.8 )
DBH c.1024+192T>C ( ENST00000393056.8 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000787.4(DBH):c.1024+192T>C AND not provided
- ClinVar Allele ID
- 1230520
- ClinVar RefSeq Alternation Syntax
- NM_000787.4:c.1024+192T>C
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-05-11
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001643465
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs