ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.793G>T (p.Ala265Ser)

dbSNP: rs2130095011
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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 RCV001977342 SCV002266831 uncertain significance Werner syndrome 2021-08-27 criteria provided, single submitter clinical testing

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