Annotation Detail
Information
- Associated Genes
- TERT LOC110806263
- Associated Variants
-
TERT c.-1382T>C
TERT c.-1382T>C - Associated Disease
- Coronary artery disease, susceptibility to
- Source Database
- ClinVar
- Description
- NM_198253.2(TERT):c.-1382T>C AND Coronary artery disease, susceptibility to
- ClinVar Allele ID
- 362290
- Clinical Significance Description
- Uncertain significance
- Clinical Significance Last Update
- 2006-09-22
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001787099
- ClinVar Disease
- Coronary artery disease, susceptibility to
- Observed Origin Sample
- germline
- Pubmed
- 16890917
Drugs