ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.2013C>T (p.His671=)

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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 RCV002876813 SCV003236366 likely benign Werner syndrome 2022-11-22 criteria provided, single submitter clinical testing

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