ClinVar Miner

Submissions for variant NM_001376.5(DYNC1H1):c.1012G>A (p.Asp338Asn)

dbSNP: rs1555408131
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
Inherited Neuropathy Consortium RCV000789732 SCV000929109 uncertain significance Neuronopathy, distal hereditary motor, autosomal dominant no assertion criteria provided literature only
Inherited Neuropathy Consortium Ii, University Of Miami RCV003447241 SCV004174348 uncertain significance Charcot-Marie-Tooth disease axonal type 2O 2016-01-06 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.