List of variants in gene CHEK2 reported as benign for not specified

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: 24

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_007194.4(CHEK2):c.252A>G (p.Glu84=)	rs1805129	0.04009
NM_007194.4(CHEK2):c.1542+11T>A	rs17881716	0.01583
NM_007194.4(CHEK2):c.1343T>G (p.Ile448Ser)	rs17886163	0.00555
NM_007194.4(CHEK2):c.593-14C>T	rs145754558	0.00235
NM_007194.4(CHEK2):c.254C>T (p.Pro85Leu)	rs17883862	0.00201
NM_007194.4(CHEK2):c.1407G>A (p.Val469=)	rs17881378	0.00190
NM_007194.4(CHEK2):c.-40G>T	rs142541707	0.00155
NM_007194.4(CHEK2):c.320-5T>A	rs121908700	0.00070
NM_007194.4(CHEK2):c.-6G>A	rs376995740	0.00065
NM_007194.4(CHEK2):c.*18C>T	rs17884403	0.00037
NM_007194.4(CHEK2):c.1176G>A (p.Ala392=)	rs142692907	0.00034
NM_007194.4(CHEK2):c.1497G>C (p.Leu499=)	rs587780890	0.00032
NM_007194.4(CHEK2):c.444+19T>C	rs200501745	0.00026
NM_007194.4(CHEK2):c.410G>A (p.Arg137Gln)	rs368570187	0.00012
NM_007194.4(CHEK2):c.1008+13C>T	rs193264230	0.00011
NM_007194.4(CHEK2):c.*7T>C	rs121908710	0.00009
NM_007194.4(CHEK2):c.1023C>T (p.Asn341=)	rs377668478	0.00006
NM_007194.4(CHEK2):c.1260-10C>G	rs730881706	0.00006
NM_007194.4(CHEK2):c.847-17T>C	rs199780411	0.00006
NM_007194.4(CHEK2):c.847-10C>G	rs745745105	0.00004
NM_007194.4(CHEK2):c.1130A>G (p.Glu377Gly)	rs560973106	0.00003
NM_007194.4(CHEK2):c.1462-7C>G	rs730881707	0.00002
NM_007194.4(CHEK2):c.528G>C (p.Gly176=)	rs587780889	0.00001
NM_007194.4(CHEK2):c.231CCAAGAACCTGAGGA[1] (p.77DQEPE[1])	rs587780181

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.