ClinVar Miner

List of variants in gene NOD2 reported as likely benign for Blau syndrome; Inflammatory bowel disease 1

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Total variants: 12
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HGVS dbSNP
NM_022162.3(NOD2):c.1172G>A (p.Arg391His) rs554887705
NM_022162.3(NOD2):c.126C>T (p.Val42=) rs766815592
NM_022162.3(NOD2):c.1280C>T (p.Pro427Leu) rs766651775
NM_022162.3(NOD2):c.1578C>G (p.Thr526=) rs779950802
NM_022162.3(NOD2):c.1836G>A (p.Ala612=) rs756626309
NM_022162.3(NOD2):c.2107C>T (p.Arg703Cys) rs5743277
NM_022162.3(NOD2):c.2264C>T (p.Ala755Val) rs61747625
NM_022162.3(NOD2):c.2733G>A (p.Val911=) rs1359941511
NM_022162.3(NOD2):c.2753C>A (p.Ala918Asp) rs104895452
NM_022162.3(NOD2):c.374C>T (p.Pro125Leu) rs149390911
NM_022162.3(NOD2):c.566C>T (p.Thr189Met) rs61755182
NM_022162.3(NOD2):c.921G>A (p.Thr307=) rs376601025

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