ClinVar Miner

Submissions for variant NM_032977.4(CASP10):c.685-20C>T

gnomAD frequency: 0.03338  dbSNP: rs17860401
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
Labcorp Genetics (formerly Invitae), Labcorp RCV001796906 SCV001727499 benign Autoimmune lymphoproliferative syndrome type 2A 2024-01-31 criteria provided, single submitter clinical testing
GeneDx RCV001655772 SCV001862505 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001655772 SCV005238004 benign not provided criteria provided, single submitter not provided

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.