List of variants in gene GLDC reported as 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_000170.3(GLDC):c.*7G>C	rs2228098	0.66615
NM_000170.3(GLDC):c.501G>A (p.Glu167=)	rs35374927	0.22564
NM_000170.3(GLDC):c.249G>A (p.Gly83=)	rs12341698	0.21682
NM_000170.3(GLDC):c.666T>C (p.Asp222=)	rs12004164	0.02547
NM_000170.3(GLDC):c.671G>A (p.Arg224His)	rs28617412	0.02214
NM_000170.3(GLDC):c.2380G>A (p.Ala794Thr)	rs141933811	0.00728
NM_000170.3(GLDC):c.319A>G (p.Met107Val)	rs138454333	0.00707
NM_000170.3(GLDC):c.1229G>A (p.Arg410Lys)	rs144090917	0.00234
NM_000170.3(GLDC):c.1156-7C>G	rs150095531	0.00208
NM_000170.3(GLDC):c.2988G>C (p.Gln996His)	rs138640017	0.00112
NM_000170.3(GLDC):c.936C>T (p.Ile312=)	rs79057118	0.00058
NM_000170.3(GLDC):c.63C>A (p.Arg21=)	rs372141443	0.00001
NM_000170.3(GLDC):c.1545G>A (p.Arg515=)	rs121964976
NM_000170.3(GLDC):c.2316-6dup	rs3215923

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.