Annotation Detail
Information
- Associated Genes
- CDKN2B CDKN2B-AS1
- Associated Variants
-
CDKN2B c.*2619C>T
(
ENST00000276925.7 )
CDKN2B c.*2619C>T ( ENST00000276925.7 ) - Associated Disease
- Three Vessel Coronary Disease
- Source Database
- ClinVar
- Description
- NM_004936.4(CDKN2B):c.*2619C>T AND Three Vessel Coronary Disease
- ClinVar Allele ID
- 800881
- ClinVar RefSeq Alternation Syntax
- NM_078487.2:c.*2922C>T
- ClinVar RefSeq Alternation Syntax
- NM_004936.4:c.*2619C>T
- Clinical Significance Description
- protective
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001003457
- ClinVar Disease
- Three Vessel Coronary Disease
- Observed Origin Sample
- somatic
Drugs