List of variants in gene JAG1 reported as benign by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 18

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000214.3(JAG1):c.3417T>C (p.Tyr1139=)	rs1051419	0.71278
NM_000214.3(JAG1):c.440-15T>C	rs2273060	0.42936
NM_000214.3(JAG1):c.765C>T (p.Tyr255=)	rs1131695	0.42930
NM_000214.3(JAG1):c.3528C>T (p.Tyr1176=)	rs1051421	0.21993
NM_000214.3(JAG1):c.588C>T (p.Cys196=)	rs1801138	0.10620
NM_000214.3(JAG1):c.2214A>C (p.Thr738=)	rs1801140	0.08777
NM_000214.3(JAG1):c.267G>A (p.Gly89=)	rs1051415	0.08298
NM_000214.3(JAG1):c.2382C>T (p.Ser794=)	rs56225585	0.07991
NM_000214.3(JAG1):c.744A>G (p.Pro248=)	rs10485741	0.06845
NM_000214.3(JAG1):c.924C>T (p.Asn308=)	rs45575136	0.02472
NM_000214.3(JAG1):c.2766C>T (p.Asp922=)	rs2229895	0.01701
NM_000214.3(JAG1):c.2573-16C>T	rs112196689	0.00568
NM_000214.3(JAG1):c.1578C>T (p.Ile526=)	rs1801139	0.00092
NM_000214.3(JAG1):c.1349-11T>G	rs80338240	0.00076
NM_000214.3(JAG1):c.894T>C (p.Asn298=)	rs149897344	0.00039
NM_000214.3(JAG1):c.2344+15C>G	rs200139177	0.00029
NM_000214.3(JAG1):c.2458+16G>A	rs772170740
NM_000214.3(JAG1):c.294C>T (p.Ser98=)	rs79338570

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.