ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.2642C>T (p.Thr881Ile)

dbSNP: rs2130342542
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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 RCV001973075 SCV002248814 uncertain significance Werner syndrome 2021-08-20 criteria provided, single submitter clinical testing

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