ClinVar Miner

Submissions for variant NM_016356.5(DCDC2):c.1271A>C (p.Gln424Pro)

dbSNP: rs794729665
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
Centre de Biotechnologie de Sfax, Université de Sfax RCV000157618 SCV000188610 pathogenic Nonsyndromic Deafness 2014-10-01 no assertion criteria provided research
OMIM RCV000185587 SCV000238481 pathogenic Autosomal recessive nonsyndromic hearing loss 66 2015-01-18 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.