Annotation Detail
Information
- Associated Genes
- CYP1A2 LOC110467516
- Associated Variants
-
CYP1A2 c.-9-154C>A
(
ENST00000343932.5 )
CYP1A2 c.-9-154C>A ( ENST00000343932.5 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000761.5(CYP1A2):c.-9-154C>A AND not specified
- ClinVar Allele ID
- 505375
- ClinVar RefSeq Alternation Syntax
- NM_000761.5:c.-9-154C>A
- 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/RCV000607978
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs