ClinVar Miner

Submissions for variant NM_001005360.2(DNM2):c.2201A>G (p.Asn734Ser) (rs577767034)

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
Athena Diagnostics Inc RCV000516555 SCV000613152 benign not specified 2016-09-01 criteria provided, single submitter clinical testing
GeneDx RCV000841305 SCV000983266 benign not provided 2021-06-04 criteria provided, single submitter clinical testing
Invitae RCV001088080 SCV001009761 benign Charcot-Marie-Tooth disease, dominant intermediate B 2020-11-16 criteria provided, single submitter clinical testing
CeGaT Praxis fuer Humangenetik Tuebingen RCV000841305 SCV001151635 uncertain significance not provided 2018-04-01 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.