ClinVar Miner

List of variants in gene NOD2 reported as uncertain significance for Inflammatory bowel disease 1

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 76
Download table as spreadsheet
HGVS dbSNP
NM_001370466.1(NOD2):c.*1013A>G
NM_001370466.1(NOD2):c.*1200A>G
NM_001370466.1(NOD2):c.*1201T>A rs751525993
NM_001370466.1(NOD2):c.*183C>T
NM_001370466.1(NOD2):c.*186C>G rs886052045
NM_001370466.1(NOD2):c.*325G>A rs886052046
NM_001370466.1(NOD2):c.*382C>T rs535063121
NM_001370466.1(NOD2):c.*394C>T rs886052048
NM_001370466.1(NOD2):c.*422C>G rs886052049
NM_001370466.1(NOD2):c.*462C>A rs562972090
NM_001370466.1(NOD2):c.*470C>T rs770461687
NM_001370466.1(NOD2):c.*609C>T
NM_001370466.1(NOD2):c.*64G>C
NM_001370466.1(NOD2):c.*873C>T rs373812846
NM_001370466.1(NOD2):c.*89C>T rs184545855
NM_001370466.1(NOD2):c.*8G>A rs199475923
NM_001370466.1(NOD2):c.-8-2193G>A rs886052043
NM_001370466.1(NOD2):c.-8-2202A>G
NM_001370466.1(NOD2):c.-8-2297C>T rs188341692
NM_001370466.1(NOD2):c.1109C>T (p.Pro370Leu) rs150078153
NM_001370466.1(NOD2):c.1188G>A (p.Val396=) rs77966199
NM_001370466.1(NOD2):c.1200G>A (p.Pro400=) rs104895430
NM_001370466.1(NOD2):c.1211C>T (p.Ser404Leu) rs104895431
NM_001370466.1(NOD2):c.1214C>T (p.Ala405Val) rs2076754
NM_001370466.1(NOD2):c.1235G>A (p.Arg412His) rs143110172
NM_001370466.1(NOD2):c.1240G>A (p.Glu414Lys) rs104895432
NM_001370466.1(NOD2):c.1428G>A (p.Glu476=) rs104895434
NM_001370466.1(NOD2):c.1510G>T (p.Ala504Ser)
NM_001370466.1(NOD2):c.1522C>T (p.Leu508=) rs145190613
NM_001370466.1(NOD2):c.1553C>T (p.Pro518Leu) rs777949388
NM_001370466.1(NOD2):c.1745T>G (p.Phe582Cys) rs777798807
NM_001370466.1(NOD2):c.1758C>T (p.Phe586=) rs149870902
NM_001370466.1(NOD2):c.1775C>T (p.Ala592Val) rs867131858
NM_001370466.1(NOD2):c.1900G>C (p.Ala634Pro) rs369957746
NM_001370466.1(NOD2):c.1922C>T (p.Pro641Leu) rs5743275
NM_001370466.1(NOD2):c.193G>A (p.Val65Ile) rs187264529
NM_001370466.1(NOD2):c.2066G>A (p.Arg689His) rs200035357
NM_001370466.1(NOD2):c.2087C>T (p.Pro696Leu) rs201076024
NM_001370466.1(NOD2):c.2149C>T (p.Arg717Trp) rs140876663
NM_001370466.1(NOD2):c.2249C>A (p.Thr750Asn) rs756184386
NM_001370466.1(NOD2):c.2251G>A (p.Glu751Lys) rs104895443
NM_001370466.1(NOD2):c.2284C>T (p.Leu762Phe) rs773758818
NM_001370466.1(NOD2):c.2290C>T (p.Arg764Trp) rs104895484
NM_001370466.1(NOD2):c.232G>A (p.Ala78Thr)
NM_001370466.1(NOD2):c.2382-9T>A rs201759367
NM_001370466.1(NOD2):c.2408G>A (p.Arg803Gln) rs770915641
NM_001370466.1(NOD2):c.2413A>G (p.Ile805Val) rs765335094
NM_001370466.1(NOD2):c.2465+1G>A rs373550987
NM_001370466.1(NOD2):c.247G>A (p.Ala83Thr)
NM_001370466.1(NOD2):c.2551C>T (p.Leu851=) rs886052044
NM_001370466.1(NOD2):c.2631G>A (p.Leu877=) rs142559533
NM_001370466.1(NOD2):c.2641G>T (p.Gly881Cys) rs2066845
NM_001370466.1(NOD2):c.2659G>A (p.Glu887Lys) rs758913334
NM_001370466.1(NOD2):c.2736T>C (p.Ile912=) rs104895454
NM_001370466.1(NOD2):c.2781C>T (p.Asn927=)
NM_001370466.1(NOD2):c.2839T>C (p.Ser947Pro)
NM_001370466.1(NOD2):c.2852G>A (p.Gly951Glu) rs104895457
NM_001370466.1(NOD2):c.3013G>A (p.Gly1005Ser) rs147874812
NM_001370466.1(NOD2):c.379G>A (p.Asp127Asn) rs146054564
NM_001370466.1(NOD2):c.403G>A (p.Val135Ile) rs139571975
NM_001370466.1(NOD2):c.435G>C (p.Leu145Phe)
NM_001370466.1(NOD2):c.450G>A (p.Pro150=) rs775281342
NM_001370466.1(NOD2):c.509C>A (p.Ala170Asp)
NM_001370466.1(NOD2):c.552C>T (p.Ala184=) rs5743269
NM_001370466.1(NOD2):c.572C>T (p.Thr191Ile)
NM_001370466.1(NOD2):c.59C>T (p.Ser20Leu) rs201586544
NM_001370466.1(NOD2):c.605C>T (p.Thr202Met)
NM_001370466.1(NOD2):c.726G>A (p.Pro242=) rs369766454
NM_001370466.1(NOD2):c.747G>A (p.Leu249=) rs763504952
NM_001370466.1(NOD2):c.760C>T (p.Leu254Phe) rs756943416
NM_001370466.1(NOD2):c.778C>T (p.His260Tyr) rs560242309
NM_001370466.1(NOD2):c.789C>T (p.Asp263=) rs749180535
NM_001370466.1(NOD2):c.794C>T (p.Ala265Val) rs149338478
NM_001370466.1(NOD2):c.800C>G (p.Thr267Ser) rs104895425
NM_001370466.1(NOD2):c.850C>T (p.Arg284Trp) rs104895427
NM_001370466.1(NOD2):c.989A>C (p.Asp330Ala) rs104895469

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.