ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.4167G>A (p.Lys1389=)

dbSNP: rs889300977
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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 RCV000866324 SCV001007403 likely benign Werner syndrome 2024-04-29 criteria provided, single submitter clinical testing

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