ClinVar Miner

Submissions for variant NM_000784.4(CYP27A1):c.1263+10del

dbSNP: rs765426068
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000267432 SCV000345563 uncertain significance not provided 2017-05-19 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002504025 SCV002812201 uncertain significance Cholestanol storage disease 2021-07-24 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002504025 SCV003024221 benign Cholestanol storage disease 2024-04-17 criteria provided, single submitter clinical testing

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.