List of variants in gene GYS2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_021957.4(GYS2):c.1553A>C (p.Glu518Ala)	rs150433001	0.00173
NM_021957.4(GYS2):c.1701G>A (p.Leu567=)	rs78337075	0.00092
NM_021957.4(GYS2):c.1710T>C (p.Phe570=)	rs149907949	0.00056
NM_021957.4(GYS2):c.1251C>T (p.Asn417=)	rs139882761	0.00031
NM_021957.4(GYS2):c.1063-15C>G	rs150691568	0.00016
NM_021957.4(GYS2):c.1767T>C (p.Thr589=)	rs147417298	0.00014
NM_021957.4(GYS2):c.615C>T (p.His205=)	rs569279347	0.00008
NM_021957.4(GYS2):c.750T>C (p.His250=)	rs200713752	0.00005
NM_021957.4(GYS2):c.831T>C (p.Val277=)	rs756223943	0.00004
NM_021957.4(GYS2):c.756T>C (p.Ala252=)	rs886049159	0.00002
NM_021957.4(GYS2):c.942-7del	rs537907545	0.00001
NM_021957.4(GYS2):c.1890+25del	rs36023861
NM_021957.4(GYS2):c.789A>G (p.Ala263=)	rs886038665
NM_021957.4(GYS2):c.840C>T (p.Asn280=)

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.