ClinVar Miner

Submissions for variant NM_206933.4(USH2A):c.7871del (p.Pro2624fs)

Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
Download table as spreadsheet
Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
SN ONGC Dept of Genetics and Molecular biology Vision Research Foundation RCV003389549 SCV003927129 pathogenic Usher syndrome 2022-12-31 criteria provided, single submitter research
Fulgent Genetics, Fulgent Genetics RCV005021870 SCV005641235 likely pathogenic Usher syndrome type 2A; Retinitis pigmentosa 39 2024-03-10 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.