ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.1359T>G (p.Ser453=)

dbSNP: rs1554522146
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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 RCV000633272 SCV000754489 likely benign Werner syndrome 2023-12-21 criteria provided, single submitter clinical testing

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