List of variants in gene DYNC1H1 reported as pathogenic for Charcot-Marie-Tooth disease

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

Download table as spreadsheet

HGVS	dbSNP
NM_001376.5(DYNC1H1):c.10031G>A (p.Arg3344Gln)	rs397509412
NM_001376.5(DYNC1H1):c.1792C>T (p.Arg598Cys)	rs587780564
NM_001376.5(DYNC1H1):c.2327C>T (p.Pro776Leu)	rs1057518083
NM_001376.5(DYNC1H1):c.751C>T (p.Arg251Cys)	rs879253979
NM_001376.5(DYNC1H1):c.752G>A (p.Arg251His)	rs794727634
NM_001376.5(DYNC1H1):c.917A>G (p.His306Arg)	rs387906738

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.