ClinVar Miner

Submissions for variant NM_003322.6(TULP1):c.823-17G>C

dbSNP: rs12215920
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001522084 SCV001731554 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
GeneDx RCV001522084 SCV001750685 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243282 SCV002514664 benign Leber congenital amaurosis 15 2021-12-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV002243281 SCV002514675 benign Retinitis pigmentosa 14 2021-12-05 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.