Annotation Detail
Information
- Associated Genes
- CETP
- Associated Variants
-
CETP c.118+279G>A
(
ENST00000200676.8,
ENST00000379780.6,
ENST00000566128.1 )
CETP c.118+279G>A ( ENST00000200676.8, ENST00000379780.6, ENST00000566128.1 ) - Associated Disease
- not provided
- Source Database
- ClinVar
- Description
- NM_000078.3(CETP):c.118+279G>A AND not provided
- ClinVar Allele ID
- 1228884
- ClinVar RefSeq Alternation Syntax
- NM_001286085.2:c.118+279G>A
- ClinVar RefSeq Alternation Syntax
- NM_000078.3:c.118+279G>A
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2018-08-30
- Clinical Significance Review Status
- criteria provided, single submitter
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV001637726
- ClinVar Disease
- not provided
- Observed Origin Sample
- germline
Drugs