ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.2937T>C (p.Ile979=)

dbSNP: rs147802438
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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 RCV001471924 SCV001676047 likely benign Werner syndrome 2024-04-10 criteria provided, single submitter clinical testing

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