ClinVar Miner

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

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Gene type:
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Total variants: 69
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HGVS dbSNP
NM_001370466.1(NOD2):c.-8-2174C>T rs149122717
NM_001370466.1(NOD2):c.-8-2185C>T rs144993105
NM_001370466.1(NOD2):c.-8-2232G>C rs140977130
NM_001370466.1(NOD2):c.1041C>T (p.Val347=) rs757517796
NM_001370466.1(NOD2):c.1091G>A (p.Arg364His) rs554887705
NM_001370466.1(NOD2):c.1110G>A (p.Pro370=) rs766883774
NM_001370466.1(NOD2):c.1188G>A (p.Val396=) rs77966199
NM_001370466.1(NOD2):c.1199C>T (p.Pro400Leu) rs766651775
NM_001370466.1(NOD2):c.1200G>C (p.Pro400=) rs104895430
NM_001370466.1(NOD2):c.1203C>T (p.Ala401=) rs547826765
NM_001370466.1(NOD2):c.1211C>T (p.Ser404Leu) rs104895431
NM_001370466.1(NOD2):c.1212G>T (p.Ser404=) rs145834617
NM_001370466.1(NOD2):c.1230C>T (p.Tyr410=) rs771979324
NM_001370466.1(NOD2):c.1235G>A (p.Arg412His) rs143110172
NM_001370466.1(NOD2):c.1239C>T (p.Thr413=) rs143395754
NM_001370466.1(NOD2):c.1242G>A (p.Glu414=) rs1224862712
NM_001370466.1(NOD2):c.1245C>T (p.Phe415=) rs151315883
NM_001370466.1(NOD2):c.1293G>A (p.Lys431=) rs1430003119
NM_001370466.1(NOD2):c.1308C>T (p.Pro436=) rs200656015
NM_001370466.1(NOD2):c.1428G>A (p.Glu476=) rs104895434
NM_001370466.1(NOD2):c.1497C>G (p.Thr499=) rs779950802
NM_001370466.1(NOD2):c.1563G>A (p.Leu521=) rs369085294
NM_001370466.1(NOD2):c.1608C>T (p.Tyr536=) rs111608429
NM_001370466.1(NOD2):c.1693G>A (p.Val565Met) rs148683734
NM_001370466.1(NOD2):c.1710G>A (p.Ala570=) rs140312093
NM_001370466.1(NOD2):c.1755G>A (p.Ala585=) rs756626309
NM_001370466.1(NOD2):c.1848C>T (p.Leu616=) rs764199623
NM_001370466.1(NOD2):c.1857G>A (p.Thr619=) rs762058298
NM_001370466.1(NOD2):c.1875G>A (p.Ser625=) rs141355588
NM_001370466.1(NOD2):c.1906C>T (p.Leu636=) rs762922997
NM_001370466.1(NOD2):c.1923G>A (p.Pro641=) rs199475914
NM_001370466.1(NOD2):c.192C>T (p.Thr64=) rs146923251
NM_001370466.1(NOD2):c.1965G>T (p.Leu655Phe) rs149002807
NM_001370466.1(NOD2):c.1970G>A (p.Arg657Gln) rs114664276
NM_001370466.1(NOD2):c.2026C>T (p.Arg676Cys) rs5743277
NM_001370466.1(NOD2):c.2130C>T (p.Pro710=) rs769210593
NM_001370466.1(NOD2):c.2139C>A (p.Ile713=) rs104895441
NM_001370466.1(NOD2):c.216C>T (p.Ala72=) rs1398956455
NM_001370466.1(NOD2):c.2183C>T (p.Ala728Val) rs61747625
NM_001370466.1(NOD2):c.2223G>A (p.Lys741=) rs1596871165
NM_001370466.1(NOD2):c.2295C>T (p.Pro765=) rs5743280
NM_001370466.1(NOD2):c.2296G>A (p.Val766Met) rs104895444
NM_001370466.1(NOD2):c.2382-9T>A rs201759367
NM_001370466.1(NOD2):c.2389G>A (p.Asp797Asn) rs61755272
NM_001370466.1(NOD2):c.255C>A (p.Ala85=) rs770046355
NM_001370466.1(NOD2):c.2586A>C (p.Gln862His) rs764244331
NM_001370466.1(NOD2):c.2652G>A (p.Val884=) rs1359941511
NM_001370466.1(NOD2):c.2658C>T (p.Asp886=) rs104895451
NM_001370466.1(NOD2):c.2672C>A (p.Ala891Asp) rs104895452
NM_001370466.1(NOD2):c.2717+158C>T rs5743289
NM_001370466.1(NOD2):c.2721G>A (p.Leu907=) rs149691662
NM_001370466.1(NOD2):c.2881C>T (p.Leu961=) rs1596908135
NM_001370466.1(NOD2):c.2931G>A (p.Leu977=) rs773388366
NM_001370466.1(NOD2):c.293C>T (p.Pro98Leu) rs149390911
NM_001370466.1(NOD2):c.2979G>A (p.Gly993=) rs374689495
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.45C>T (p.Val15=) rs766815592
NM_001370466.1(NOD2):c.485C>T (p.Thr162Met) rs61755182
NM_001370466.1(NOD2):c.510C>T (p.Ala170=) rs765729513
NM_001370466.1(NOD2):c.606G>A (p.Thr202=) rs771003092
NM_001370466.1(NOD2):c.760C>T (p.Leu254Phe) rs756943416
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.840G>A (p.Thr280=) rs376601025
NM_001370466.1(NOD2):c.850C>T (p.Arg284Trp) rs104895427
NM_001370466.1(NOD2):c.9G>A (p.Ser3=) rs774491311
NM_022162.2(NOD2):c.241C>G (p.Leu81Val) rs34936594

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