ClinVar Miner

Submissions for variant NM_001370466.1(NOD2):c.2633+12T>C

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV003803735 SCV004593818 likely benign Blau syndrome; Regional enteritis 2024-12-04 criteria provided, single submitter clinical testing

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