ClinVar Miner

Submissions for variant NM_006015.6(ARID1A):c.3898_3899del (p.Met1300fs)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
MGZ Medical Genetics Center RCV002288421 SCV002580776 likely pathogenic Intellectual disability, autosomal dominant 14 2022-02-16 criteria provided, single submitter clinical testing

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