ClinVar Miner

Submissions for variant NM_032776.3(JMJD1C):c.1919del (p.Pro640fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Equipe Genetique des Anomalies du Developpement, Université de Bourgogne RCV003151944 SCV003840248 uncertain significance TELO2-related intellectual disability-neurodevelopmental disorder 2021-01-04 criteria provided, single submitter research

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