ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.2379A>G (p.Thr793=)

dbSNP: rs1801525077
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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 RCV001345280 SCV001539387 likely benign Werner syndrome 2024-02-24 criteria provided, single submitter clinical testing

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