ClinVar Miner

Submissions for variant NM_001029871.4(RSPO4):c.98dup (p.Asn34fs)

dbSNP: rs768138495
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Center for Genomic Medicine, King Faisal Specialist Hospital and Research Center RCV000001253 SCV004805979 uncertain significance Anonychia 2024-03-25 criteria provided, single submitter clinical testing
OMIM RCV000001253 SCV000021403 pathogenic Anonychia 2006-12-01 no assertion criteria provided literature only

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.