ClinVar Miner

Submissions for variant NM_001111125.3(IQSEC2):c.2582+19C>T

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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 RCV005074821 SCV005701186 likely benign Intellectual disability, X-linked 1 2024-12-02 criteria provided, single submitter clinical testing

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