ClinVar Miner

List of variants in gene NOD2 reported as benign

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Gene type:
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Total variants: 26
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HGVS dbSNP
NM_022162.3(NOD2):c.*1156G>A rs3135500
NM_022162.3(NOD2):c.*397A>C rs3135499
NM_022162.3(NOD2):c.-59G>A rs2076752
NM_022162.3(NOD2):c.1055A>G (p.His352Arg) rs5743272
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.1377C>T (p.Arg459=) rs2066843
NM_022162.3(NOD2):c.1453C>T (p.Leu485=) rs5743274
NM_022162.3(NOD2):c.1761T>G (p.Arg587=) rs1861759
NM_022162.3(NOD2):c.1788G>A (p.Thr596=) rs104895437
NM_022162.3(NOD2):c.1833C>T (p.Ala611=) rs61736932
NM_022162.3(NOD2):c.2104C>T (p.Arg702Trp) rs2066844
NM_022162.3(NOD2):c.2123G>A (p.Arg708His) rs35285618
NM_022162.3(NOD2):c.2174C>G (p.Ala725Gly) rs5743278
NM_022162.3(NOD2):c.2369G>A (p.Arg790Gln) rs5743279
NM_022162.3(NOD2):c.2372G>A (p.Arg791Gln) rs104895464
NM_022162.3(NOD2):c.2587A>G (p.Met863Val) rs104895447
NM_022162.3(NOD2):c.2863G>A (p.Val955Ile) rs5743291
NM_022162.3(NOD2):c.418G>A (p.Ala140Thr) rs34684955
NM_022162.3(NOD2):c.534C>G (p.Ser178=) rs2067085
NM_022162.3(NOD2):c.541-3T>C rs141833420
NM_022162.3(NOD2):c.74-7T>A rs104895421
NM_022162.3(NOD2):c.743T>G (p.Leu248Arg) rs104895423
NM_022162.3(NOD2):c.802C>T (p.Pro268Ser) rs2066842
NM_022162.3(NOD2):c.816C>T (p.Ser272=) rs35090774
NM_022162.3(NOD2):c.866A>G (p.Asn289Ser) rs5743271

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