ClinVar Miner

Submissions for variant CYP2C19*13/*27

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Clinical Pharmacogenetics Implementation Consortium RCV000782813 SCV000921336 drug response Citalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000782814 SCV000921337 drug response Escitalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000783234 SCV000921757 drug response Sertraline response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000784613 SCV000923136 drug response Voriconazole response practice guideline curation

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.