ClinVar Miner

List of variants studied for Crohn disease

Included ClinVar conditions (1):
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ClinVar version:
Total variants: 96
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HGVS dbSNP
NM_022162.3(NOD2):c.*1023C>T rs5743299
NM_022162.3(NOD2):c.*1156G>A rs3135500
NM_022162.3(NOD2):c.*1201T>A rs751525993
NM_022162.3(NOD2):c.*186C>G rs886052045
NM_022162.3(NOD2):c.*325G>A rs886052046
NM_022162.3(NOD2):c.*329_*334dup rs886052047
NM_022162.3(NOD2):c.*382C>T rs535063121
NM_022162.3(NOD2):c.*394C>T rs886052048
NM_022162.3(NOD2):c.*397A>C rs3135499
NM_022162.3(NOD2):c.*422C>G rs886052049
NM_022162.3(NOD2):c.*462C>A rs562972090
NM_022162.3(NOD2):c.*470C>T rs770461687
NM_022162.3(NOD2):c.*521C>T rs5743297
NM_022162.3(NOD2):c.*620G>A rs116213743
NM_022162.3(NOD2):c.*873C>T rs373812846
NM_022162.3(NOD2):c.*877C>A rs140643942
NM_022162.3(NOD2):c.*89C>T rs184545855
NM_022162.3(NOD2):c.*990T>C rs192842874
NM_022162.3(NOD2):c.-14C>T rs117611225
NM_022162.3(NOD2):c.-53C>T rs188341692
NM_022162.3(NOD2):c.-58T>C rs139485985
NM_022162.3(NOD2):c.-59G>A rs2076752
NM_022162.3(NOD2):c.-96del rs5743265
NM_022162.3(NOD2):c.1172G>A (p.Arg391His) rs554887705
NM_022162.3(NOD2):c.1269G>T (p.Val423=) rs77966199
NM_022162.3(NOD2):c.1281G>A (p.Pro427=) rs104895430
NM_022162.3(NOD2):c.1292C>T (p.Ser431Leu) rs104895431
NM_022162.3(NOD2):c.1316G>A (p.Arg439His) rs143110172
NM_022162.3(NOD2):c.1377C>T (p.Arg459=) rs2066843
NM_022162.3(NOD2):c.140C>T (p.Ser47Leu) rs201586544
NM_022162.3(NOD2):c.1411C>T (p.Arg471Cys) rs1078327
NM_022162.3(NOD2):c.1509G>A (p.Glu503=) rs104895434
NM_022162.3(NOD2):c.1603C>T (p.Leu535=) rs145190613
NM_022162.3(NOD2):c.1634C>T (p.Pro545Leu) rs777949388
NM_022162.3(NOD2):c.1689C>T (p.Tyr563=) rs111608429
NM_022162.3(NOD2):c.1761T>G (p.Arg587=) rs1861759
NM_022162.3(NOD2):c.1833C>T (p.Ala611=) rs61736932
NM_022162.3(NOD2):c.1834G>A (p.Ala612Thr) rs104895438
NM_022162.3(NOD2):c.1834G>T (p.Ala612Ser) rs104895438
NM_022162.3(NOD2):c.1839C>T (p.Phe613=) rs149870902
NM_022162.3(NOD2):c.1856C>T (p.Ala619Val) rs867131858
NM_022162.3(NOD2):c.1981G>C (p.Ala661Pro) rs369957746
NM_022162.3(NOD2):c.2003C>T (p.Pro668Leu) rs5743275
NM_022162.3(NOD2):c.2046G>T (p.Leu682Phe) rs149002807
NM_022162.3(NOD2):c.2050C>T (p.Arg684Trp) rs5743276
NM_022162.3(NOD2):c.2104C>T (p.Arg702Trp) rs2066844
NM_022162.3(NOD2):c.2107C>T (p.Arg703Cys) rs5743277
NM_022162.3(NOD2):c.2123G>A (p.Arg708His) rs35285618
NM_022162.3(NOD2):c.2147G>A (p.Arg716His) rs200035357
NM_022162.3(NOD2):c.2174C>G (p.Ala725Gly) rs5743278
NM_022162.3(NOD2):c.2264C>T (p.Ala755Val) rs61747625
NM_022162.3(NOD2):c.2330C>A (p.Thr777Asn) rs756184386
NM_022162.3(NOD2):c.2365C>T (p.Leu789Phe) rs773758818
NM_022162.3(NOD2):c.2372G>A (p.Arg791Gln) rs104895464
NM_022162.3(NOD2):c.2377G>A (p.Val793Met) rs104895444
NM_022162.3(NOD2):c.2406G>T (p.Val802=) rs104895495
NM_022162.3(NOD2):c.2462+10A>C rs72796353
NM_022162.3(NOD2):c.2463-9T>A rs201759367
NM_022162.3(NOD2):c.2489G>A (p.Arg830Gln) rs770915641
NM_022162.3(NOD2):c.2494A>G (p.Ile832Val) rs765335094
NM_022162.3(NOD2):c.2546C>T (p.Ala849Val) rs104895486
NM_022162.3(NOD2):c.2547-11G>T rs5743285
NM_022162.3(NOD2):c.2555A>G (p.Asn852Ser) rs104895467
NM_022162.3(NOD2):c.2587A>G (p.Met863Val) rs104895447
NM_022162.3(NOD2):c.2632C>T (p.Leu878=) rs886052044
NM_022162.3(NOD2):c.2704C>A (p.Gln902Lys) rs201035873
NM_022162.3(NOD2):c.2712G>A (p.Leu904=) rs142559533
NM_022162.3(NOD2):c.2722G>C (p.Gly908Arg) rs2066845
NM_022162.3(NOD2):c.2740G>A (p.Glu914Lys) rs758913334
NM_022162.3(NOD2):c.274G>A (p.Val92Ile) rs187264529
NM_022162.3(NOD2):c.2753C>A (p.Ala918Asp) rs104895452
NM_022162.3(NOD2):c.2863G>A (p.Val955Ile) rs5743291
NM_022162.3(NOD2):c.3019dup (p.Leu1007fs) rs2066847
NM_022162.3(NOD2):c.3094G>A (p.Gly1032Ser) rs147874812
NM_022162.3(NOD2):c.413G>A (p.Arg138Gln) rs104895456
NM_022162.3(NOD2):c.460G>A (p.Asp154Asn) rs146054564
NM_022162.3(NOD2):c.484G>A (p.Val162Ile) rs139571975
NM_022162.3(NOD2):c.52G>A (p.Val18Ile) rs886052043
NM_022162.3(NOD2):c.531G>A (p.Pro177=) rs775281342
NM_022162.3(NOD2):c.534C>G (p.Ser178=) rs2067085
NM_022162.3(NOD2):c.541-3T>C rs141833420
NM_022162.3(NOD2):c.566C>T (p.Thr189Met) rs61755182
NM_022162.3(NOD2):c.633C>T (p.Ala211=) rs5743269
NM_022162.3(NOD2):c.646+15T>C rs765487015
NM_022162.3(NOD2):c.703C>T (p.Arg235Cys) rs104895422
NM_022162.3(NOD2):c.734C>T (p.Thr245Met) rs148516118
NM_022162.3(NOD2):c.74-7T>A rs104895421
NM_022162.3(NOD2):c.802C>T (p.Pro268Ser) rs2066842
NM_022162.3(NOD2):c.807G>A (p.Pro269=) rs369766454
NM_022162.3(NOD2):c.828G>A (p.Leu276=) rs763504952
NM_022162.3(NOD2):c.841C>T (p.Leu281Phe) rs756943416
NM_022162.3(NOD2):c.859C>T (p.His287Tyr) rs560242309
NM_022162.3(NOD2):c.866A>G (p.Asn289Ser) rs5743271
NM_022162.3(NOD2):c.875C>T (p.Ala292Val) rs149338478
NM_022162.3(NOD2):c.881C>G (p.Thr294Ser) rs104895425
NM_022162.3(NOD2):c.931C>T (p.Arg311Trp) rs104895427

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