ClinVar Miner

Submissions for variant NM_001145026.2(PTPRQ):c.1882+16TTG[7]

dbSNP: rs58537253
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
GeneDx RCV001645738 SCV001858884 benign not provided 2019-11-14 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796633 SCV002033314 benign Hearing loss, autosomal dominant 73 2021-11-07 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001796632 SCV002033315 benign Autosomal recessive nonsyndromic hearing loss 84A 2021-11-07 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.