ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3139-19T>A

dbSNP: rs2130416868
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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 RCV002170580 SCV002348684 likely benign Werner syndrome 2021-03-29 criteria provided, single submitter clinical testing

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