ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.2388G>A (p.Ala796=)

dbSNP: rs1563360977
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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 RCV000706840 SCV000835914 likely benign Werner syndrome 2024-11-03 criteria provided, single submitter clinical testing

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