ClinVar Miner

Submissions for variant NM_004230.4(S1PR2):c.419A>G (p.Tyr140Cys) (rs869312750)

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
National Institute on Deafness and Communication Disorders,National Institutes of Health RCV000210070 SCV000258417 pathogenic Deafness, autosomal recessive 68 2016-01-08 no assertion criteria provided research
OMIM RCV000210070 SCV000265989 pathogenic Deafness, autosomal recessive 68 2017-10-19 no assertion criteria provided literature only

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.