List of variants reported as pathogenic for neuromuscular junction disease by Genetic Services Laboratory, University of Chicago

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

Total variants: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_005592.4(MUSK):c.79+2T>G	rs200783529	0.00004
NM_173660.5(DOK7):c.596del (p.Ile199fs)	rs797045528	0.00001
NM_000080.4(CHRNE):c.1090dup (p.Arg364fs)	rs1156634884
NM_173660.5(DOK7):c.1021_1039dup (p.Ser347fs)	rs1553850100
NM_173660.5(DOK7):c.1124_1127dup (p.Ala378fs)	rs606231128

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.