ClinVar Miner

Submissions for variant NM_025099.6(CTC1):c.225T>C (p.Thr75=)

dbSNP: rs761598220
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
Sema4, Sema4 RCV002258426 SCV002531276 likely benign Dyskeratosis congenita 2021-02-24 criteria provided, single submitter curation
Labcorp Genetics (formerly Invitae), Labcorp RCV002258426 SCV004662222 likely benign Dyskeratosis congenita 2023-12-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004706435 SCV005211638 likely 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.