Annotation Detail
Information
- Associated Genes
- ADRA2A
- Associated Variants
-
ADRA2A c.-1252G>C
ADRA2A c.-1252G>C - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000681.3(ADRA2A):c.-1252G>C AND not specified
- ClinVar Allele ID
- 502747
- 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/RCV000611315
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs