List of variants in gene GPX4 reported as benign for not provided

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: 20

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_002085.5(GPX4):c.*44T>C	rs713041	0.60751
NC_000019.10:g.1106846C>T	rs2075710	0.34577
NM_002085.5(GPX4):c.85-311C>T	rs117193629	0.04645
NM_002085.5(GPX4):c.476+36T>G	rs1224913848	0.03588
NM_002085.5(GPX4):c.476+42T>G	rs1336259165	0.03459
NM_002085.5(GPX4):c.391A>G (p.Ser131Gly)	rs73507255	0.02522
NM_002085.5(GPX4):c.179+31T>C	rs8178970	0.01604
NM_002085.5(GPX4):c.562-7C>G	rs199948868	0.00234
NM_002085.5(GPX4):c.85-284C>G	rs199515520	0.00210
NM_002085.5(GPX4):c.498C>T (p.Thr166=)	rs14283	0.00185
NM_002085.5(GPX4):c.402C>T (p.Cys134=)	rs769250904	0.00007
NM_002085.5(GPX4):c.264C>T (p.Ala88=)	rs575039682	0.00005
NC_000019.10:g.1103631dup	rs11407575
NM_002085.5(GPX4):c.324+12C>A	rs543575878
NM_002085.5(GPX4):c.324+22dup	rs147209672
NM_002085.5(GPX4):c.476+42_476+47del	rs146333943
NM_002085.5(GPX4):c.501+19del
NM_002085.5(GPX4):c.501+9del
NM_002085.5(GPX4):c.561+19G>C	rs8178977
NM_002085.5(GPX4):c.85-250G>C

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.