ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3243T>C (p.Thr1081=)

dbSNP: rs1554533018
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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 RCV001498994 SCV001703750 likely benign Werner syndrome 2019-06-30 criteria provided, single submitter clinical testing

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