ClinVar Miner

Submissions for variant NM_000553.6(WRN):c.3684T>A (p.Val1228=)

dbSNP: rs2130454749
Minimum review status: Collection method:
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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 RCV002177287 SCV002342990 likely benign Werner syndrome 2023-01-22 criteria provided, single submitter clinical testing

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