ClinVar Miner

Submissions for variant NM_022162.3(NOD2):c.2587A>G (p.Met863Val) (rs104895447)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000403018 SCV000397289 likely benign Crohn disease 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000297099 SCV000397290 likely benign Blau syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000638068 SCV000759548 benign not provided 2018-12-27 criteria provided, single submitter clinical testing
Unité médicale des maladies autoinflammatoires, CHRU Montpellier RCV000297099 SCV000116246 not provided Blau syndrome no assertion provided not provided

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