ClinVar Miner

Submissions for variant CYP2C19*7/*32

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 RCV000783026 SCV000921549 drug response Citalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000783027 SCV000921550 drug response Escitalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000784577 SCV000923100 drug response Sertraline response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000784724 SCV000923247 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.