ClinVar Miner

Submissions for variant NM_080632.3(UPF3B):c.371-9dup

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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 RCV005154313 SCV005779778 benign Syndromic X-linked intellectual disability 14 2024-02-27 criteria provided, single submitter clinical testing

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