ClinVar Miner

List of variants in gene NOD2 reported as likely benign by Invitae

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 12
Download table as spreadsheet
NM_022162.3(NOD2):c.1172G>A (p.Arg391His) rs554887705
NM_022162.3(NOD2):c.126C>T (p.Val42=) rs766815592
NM_022162.3(NOD2):c.1280C>T (p.Pro427Leu) rs766651775
NM_022162.3(NOD2):c.1578C>G (p.Thr526=) rs779950802
NM_022162.3(NOD2):c.1836G>A (p.Ala612=) rs756626309
NM_022162.3(NOD2):c.2107C>T (p.Arg703Cys) rs5743277
NM_022162.3(NOD2):c.2264C>T (p.Ala755Val) rs61747625
NM_022162.3(NOD2):c.2733G>A (p.Val911=) rs1359941511
NM_022162.3(NOD2):c.2753C>A (p.Ala918Asp) rs104895452
NM_022162.3(NOD2):c.374C>T (p.Pro125Leu) rs149390911
NM_022162.3(NOD2):c.566C>T (p.Thr189Met) rs61755182
NM_022162.3(NOD2):c.921G>A (p.Thr307=) rs376601025

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.