ClinVar Miner

Submissions for variant NM_153676.4(USH1C):c.579+61G>A

gnomAD frequency: 0.23593  dbSNP: rs72870320
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
Genome-Nilou Lab RCV001537947 SCV001754882 benign Usher syndrome type 1C 2021-07-10 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001537948 SCV001754883 benign Autosomal recessive nonsyndromic hearing loss 18A 2021-07-10 criteria provided, single submitter clinical testing
GeneDx RCV001539299 SCV001757055 benign not provided 2018-06-24 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001539299 SCV005316561 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.