ClinVar Miner

Submissions for variant CYP2C19*7/*31

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 RCV000783025 SCV000921548 drug response Escitalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000784261 SCV000922784 drug response Citalopram response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000784576 SCV000923099 drug response Sertraline response practice guideline curation
Clinical Pharmacogenetics Implementation Consortium RCV000784723 SCV000923246 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.