ClinVar Miner

List of variants in gene NOD2 reported as likely benign for not provided

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Gene type:
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Total variants: 35
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HGVS dbSNP
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.1200G>C (p.Pro400=) rs104895430
NM_001370466.1(NOD2):c.1211C>T (p.Ser404Leu) rs104895431
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.1497C>G (p.Thr499=) rs779950802
NM_001370466.1(NOD2):c.1563G>A (p.Leu521=) rs369085294
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.1906C>T (p.Leu636=) rs762922997
NM_001370466.1(NOD2):c.1923G>A (p.Pro641=) rs199475914
NM_001370466.1(NOD2):c.2130C>T (p.Pro710=) rs769210593
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.2296G>A (p.Val766Met) rs104895444
NM_001370466.1(NOD2):c.2490C>T (p.Asp830=) rs144083291
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.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.486G>A (p.Thr162=) rs144887729
NM_001370466.1(NOD2):c.510C>T (p.Ala170=) rs765729513
NM_001370466.1(NOD2):c.726G>A (p.Pro242=) rs369766454
NM_001370466.1(NOD2):c.789C>T (p.Asp263=) rs749180535
NM_001370466.1(NOD2):c.9G>A (p.Ser3=) rs774491311

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