Annotation Detail
Information
- Associated Genes
- CYP3A4 LOC110366354
- Associated Variants
-
CYP3A4 c.-392G>A
CYP3A4 c.-392G>A - Associated Disease
- Cyp3a4-v
- Source Database
- ClinVar
- Description
- NM_017460.5(CYP3A4):c.-392G>A AND Cyp3a4-v
- ClinVar Allele ID
- 31955
- Clinical Significance Description
- Benign
- Clinical Significance Last Update
- 2015-05-18
- Clinical Significance Review Status
- no assertion criteria provided
- URL
- https://www.ncbi.nlm.nih.gov/clinvar/RCV000018418
- ClinVar Disease
- Cyp3a4-v
- Observed Origin Sample
- germline
- Pubmed
- 9789061
- Pubmed
- 12107441
- Pubmed
- 10660343
- Pubmed
- 9719084
- Pubmed
- 10548319
Drugs