ClinVar Miner

Submissions for variant NM_024782.3(NHEJ1):c.369C>T (p.Cys123=)

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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 RCV003028674 SCV003321478 likely benign Cernunnos-XLF deficiency 2022-02-23 criteria provided, single submitter clinical testing

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