ClinVar Miner

Submissions for variant NM_175875.5(SIX5):c.1773G>T (p.Thr591=)

dbSNP: rs138916954
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 RCV001703275 SCV002445724 benign not provided 2024-12-06 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002506740 SCV002813071 likely benign Branchiootorenal syndrome 2 2022-03-08 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory, University Medical Center Utrecht RCV001703275 SCV001932625 likely benign not provided no assertion criteria provided clinical testing
Clinical Genetics DNA and cytogenetics Diagnostics Lab, Erasmus MC, Erasmus Medical Center RCV001703275 SCV001970032 likely benign not provided no assertion criteria provided 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.