ClinVar Miner

Submissions for variant NM_004086.3(COCH):c.153A>C (p.Pro51=)

gnomAD frequency: 0.00065  dbSNP: rs573330522
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
Eurofins Ntd Llc (ga) RCV000287205 SCV000340640 uncertain significance not provided 2016-04-15 criteria provided, single submitter clinical testing
GeneDx RCV000287205 SCV001752129 likely benign not provided 2020-11-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000287205 SCV005755583 benign not provided 2024-11-13 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV003949885 SCV004766186 likely benign COCH-related disorder 2019-12-18 no assertion criteria provided clinical testing This variant is classified as likely benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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.