Annotation Detail
Information
- Associated Genes
- CYP2C19
- Associated Variants
-
CYP2C19 p.Pro227= (p.P227=)
(
ENST00000371321.9 )
CYP2C19 p.Pro227= (p.P227=) ( ENST00000371321.9 ) - Associated Disease
- not specified
- Source Database
- ClinVar
- Description
- NM_000769.4(CYP2C19):c.681G>A (p.Pro227=) AND not specified
- ClinVar Allele ID
- 31936
- ClinVar RefSeq Alternation Syntax
- NM_000769.4:c.681G>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/RCV000610614
- ClinVar Disease
- not specified
- Observed Origin Sample
- germline
Drugs