ClinVar Miner

List of variants in gene NOD2 reported as uncertain significance for Crohn disease

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Total variants: 26
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HGVS dbSNP
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.*394C>T rs886052048
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.*873C>T rs373812846
NM_022162.3(NOD2):c.1281G>A (p.Pro427=) rs104895430
NM_022162.3(NOD2):c.140C>T (p.Ser47Leu) rs201586544
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.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.2330C>A (p.Thr777Asn) rs756184386
NM_022162.3(NOD2):c.2365C>T (p.Leu789Phe) rs773758818
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.2632C>T (p.Leu878=) rs886052044
NM_022162.3(NOD2):c.2740G>A (p.Glu914Lys) rs758913334
NM_022162.3(NOD2):c.52G>A (p.Val18Ile) rs886052043
NM_022162.3(NOD2):c.807G>A (p.Pro269=) rs369766454
NM_022162.3(NOD2):c.841C>T (p.Leu281Phe) rs756943416

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