ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.3198+2dup

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Service de Génétique Moléculaire, Hôpital Robert Debré RCV001270408 SCV001450694 likely pathogenic Intellectual disability, autosomal dominant 14 2020-07-24 no assertion criteria provided clinical testing

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