Annotation Detail
Information
- Associated Genes
- DRD1
- Associated Variants
-
DRD1 c.-48G>A
(
ENST00000393752.3 )
DRD1 c.-48G>A ( ENST00000393752.3 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000794.5(DRD1):c.-48G>A AND not specified
- ClinVar Allele ID
- 501106
- ClinVar RefSeq Alternation Syntax
- NM_000794.5:c.-48G>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/RCV000608357
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs