List of variants studied for Glycogen storage disorder due to hepatic glycogen synthase deficiency by 3billion

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 5

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_021957.4(GYS2):c.1436C>A (p.Pro479Gln)	rs121918420	0.00009
NM_021957.4(GYS2):c.736C>T (p.Arg246Ter)	rs121918419	0.00009
NM_021957.4(GYS2):c.547C>T (p.Gln183Ter)	rs201157731	0.00005
NM_021957.4(GYS2):c.841G>A (p.Gly281Ser)	rs767722149	0.00001
NM_021957.4(GYS2):c.465del (p.Phe155fs)	rs763929651

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.