Annotation Detail
Information
- Associated Genes
- DRD2
- Associated Variants
-
DRD2 c.*52G>A
(
ENST00000542968.5,
ENST00000538967.5,
ENST00000362072.8,
ENST00000346454.7,
ENST00000544518.5 )
DRD2 c.*52G>A ( ENST00000346454.7, ENST00000362072.8, ENST00000538967.5, ENST00000542968.5, ENST00000544518.5 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000795.4(DRD2):c.*52G>A AND not provided
- ClinVar Allele ID
- 1269083
- ClinVar RefSeq Alternation Syntax
- NM_000795.4:c.*52G>A
- ClinVar RefSeq Alternation Syntax
- NM_016574.4:c.*52G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2021-06-18
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001692907
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs