ClinVar Miner

Submissions for variant NM_022162.3(NOD2):c.2798+158C>T (rs5743289)

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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000004962 SCV000025138 risk factor Inflammatory bowel disease 1 2004-04-01 no assertion criteria provided literature only
OMIM RCV000416486 SCV000494282 pathogenic Blau syndrome 2004-04-01 no assertion criteria provided literature only
OMIM RCV000416489 SCV000494283 risk factor Yao syndrome 2004-04-01 no assertion criteria provided literature only

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